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| Name | Class |
|---|---|
| Business Finland | OTHER |
| Helsinki University Central Hospital | OTHER |
| Turku University Hospital | OTHER_GOV |
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The purpose of the study is to evaluate the effects of a game-based digital-therapeutics (DTx) medical software device on the symptoms of depression in adults with confirmed major depressive disorder.
The study is a comparator-controlled, randomised, double-blinded intervention study aimed at assessing the effects of the investigational device MEL-T01, "Meliora", on the symptoms of major depressive disorder (MDD). MEL-S01 acts as a comparator. MEL-T01 is a game-based digital-therapeutics (DTx) medical software device developed at Aalto University and is intended to be used as a treatment for MDD together with treatment-as-usual (TAU). MEL-T01 implements personalised cognitive training to alleviate MDD symptoms and improve cognitive performance in MDD subjects.
Subjects volunteering to participate in this investigation are adults whose MDD is confirmed through MINI interview. They have an on-going mental health treatment contact with a mental health professional. The subjects are randomised into three arms with equal probabilities in blocks of six consecutive subjects. Subjects in the MEL-T01 and MEL-S01 arms are engaged in the intervention for 12 weeks while those in the TAU arm are on a follow-up period during these 12 weeks. After this 12-week period, the subjects in MEL-T01 and MEL-S01 arms enter a 12-week follow-up period and the subjects in TAU arm engage with either the MEL-T01 or MEL-S01 intervention (randomised at T0 with equal probability) for 12 weeks.
The subjects are recommended to play the investigational-device game for a total of 48 hours during the 12 weeks of active intervention with a recommended weekly dose of 4 hours. A minimum of 24 hours is needed for inclusion to hypothesis testing. The subjects are limited to a daily maximum of 1.5 hours of game time.
The subjects' mental health symptoms and well-being are evaluated through online questionnaires five times: before subjects are randomised into one of the three groups (T0), and then 4 (T1), 8 (T2), 12 (T3), and 24 (T4) weeks after the study has begun.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| MEL-T01 | Experimental | MEL-T01 is a game-based digital-therapeutics (DTx) medical software device that implements personalised cognitive training to alleviate MDD symptoms and improve cognitive performance in MDD subjects. |
|
| MEL-S01 | Active Comparator | MEL-S01 is an active comparator similar to MEL-T01 but without personalized cognitive training elements. |
|
| TAU | No Intervention | Treatment-as-usual. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| MEL-T01 | Device | A 12 week intervention with MEL-T01. |
|
|
| Measure | Description | Time Frame |
|---|---|---|
| PHQ-9 Total Change From Baseline to Posttreatment: Experimental Group vs. Treatment as Usual Group | The patient health questionnaire (PHQ-9, Kroenke et al., 2001) is a self-report measure of major depressive disorder. The PHQ-9 scores each of the nine DSM-IV criteria for MDD from "0" (not at all) to "3" (nearly every day), providing a 0-27 severity score of depression. The higher the total score the more severe the depression. The change in the PHQ-9 total score between before the 12 week intervention and after the intervention is measured. The change score of MEL-T01 group is compared with the change score of the treatment-as-usual (TAU) group. | Day 0 to Day 84 |
| PHQ-9 Total Change From Baseline to Posttreatment: Active Comparator Group vs. Treatment as Usual Group | The patient health questionnaire (PHQ-9, Kroenke et al., 2001) is a self-report measure of major depressive disorder. The PHQ-9 scores each of the nine DSM-IV criteria for MDD from "0" (not at all) to "3" (nearly every day), providing a 0-27 severity score of depression. The higher the total score the more severe the depression. The change in the PHQ-9 total score between before the 12 week intervention and after the intervention is measured. The change score of MEL-S01 group is compared with the change score of the treatment-as-usual (TAU) group. | Day 0 to Day 84 |
| PHQ-9 Total Change From Baseline to Posttreatment: Experimental Group vs. Active Comparator Group | The patient health questionnaire (PHQ-9, Kroenke et al., 2001) is a self-report measure of major depressive disorder. The PHQ-9 scores each of the nine DSM-IV criteria for MDD from "0" (not at all) to "3" (nearly every day), providing a 0-27 severity score of depression. The higher the total score the more severe the depression. The change in the PHQ-9 total score between before the 12 week intervention and after the intervention is measured. The change score of MEL-T01 group is compared with the change score in the MEL-S01 group. | Day 0 to Day 84 |
| Measure | Description | Time Frame |
|---|---|---|
| QIDS Total Change From Baseline to Posttreatment | The quick inventory of depressive symptomatology (QIDS-SR16) is a self-report measure comprising of 16 questions on a scale of 0-3 which assess the severity of depressive symptoms. The inventory provides a total score between 0 and 48: the higher the total score the more severe the depression. For each of the three study arms, the change in total QIDS-SR16 scores between before the intervention and after the 12 week intervention is measured. Then, the average change scores in each of the three groups are compared with each other. |
| Measure | Description | Time Frame |
|---|---|---|
| GAS Total Change From Baseline to Posttreatment | The game addiction scale (GAS, Lemmens et al., 2009) is a self-report 7-item questionnaire using a 1-5 scale which measures game addiction. This provides a total between 7 and 35: the higher the scores indicate higher addiction. For each of the three study arms, the change in total GAS scores between before the intervention and after the 12 week intervention is measured. Then, the average change scores in each of the three groups are compared with each other. |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Hanna Renvall, PhD | Helsinki University Central Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Turku University Hospital | Turku | Southwest Finland | 20521 | Finland | ||
| Aalto University (TMS) |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 40165237 | Derived | Lukka L, Vesterinen M, Salonen A, Bergman VR, Torkki P, Palva S, Palva JM. User journey method: a case study for improving digital intervention use measurement. BMC Health Serv Res. 2025 Apr 1;25(1):479. doi: 10.1186/s12913-025-12641-9. |
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1,384 participants were assessed for eligibility and 1,001 were enrolled and randomized to MEL-T01, MEL-S01, or TAU. Participants randomized to TAU were further allocated at baseline to receive either MEL-T01 or MEL-S01 after the initial 12-week period.
Patients were recruited between 28th of June 2022 and 31st of December 2023. The study was conducted remotely in Finland.
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| ID | Title | Description |
|---|---|---|
| FG000 | MEL-T01 | MEL-T01 is a game-based digital-therapeutics (DTx) medical software device that implements personalised cognitive training to alleviate MDD symptoms and improve cognitive performance in MDD subjects. MEL-T01: A 12 week intervention with MEL-T01 as adjunct to TAU. |
| FG001 | MEL-S01 | MEL-S01 is an active comparator similar to MEL-T01 but without personalized cognitive training elements. MEL-S01: A 12 week intervention with MEL-S01 as adjunct to TAU. |
| FG002 | TAU (Treatment-As-Usual; First TAU, Then MEL-T01) | Treatment-as-usual in healthcare for 12 weeks. Then, the participant is given acess to MEL-T01 for 12 weeks. |
| FG003 | TAU (Treatment-As-Usual; First TAU, Then MEL-S01) | Treatment-as-usual in healthcare for 12 weeks. Then, the participant is given acess to MEL-T01 for 12 weeks. |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
Per protocol completer cohort.
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| ID | Title | Description |
|---|---|---|
| BG000 | MEL-T01 | MEL-T01 is a game-based digital-therapeutics (DTx) medical software device that implements personalised cognitive training to alleviate MDD symptoms and improve cognitive performance in MDD subjects. MEL-T01: A 12 week intervention with MEL-T01. |
| BG001 | MEL-S01 |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | PHQ-9 Total Change From Baseline to Posttreatment: Experimental Group vs. Treatment as Usual Group | The patient health questionnaire (PHQ-9, Kroenke et al., 2001) is a self-report measure of major depressive disorder. The PHQ-9 scores each of the nine DSM-IV criteria for MDD from "0" (not at all) to "3" (nearly every day), providing a 0-27 severity score of depression. The higher the total score the more severe the depression. The change in the PHQ-9 total score between before the 12 week intervention and after the intervention is measured. The change score of MEL-T01 group is compared with the change score of the treatment-as-usual (TAU) group. | Per protocol completer cohort. Analyses were restricted to weeks 0-12; TAU participants were pooled as all received identical treatment during this period, regardless of later allocation. | Posted | Least Squares Mean | 90% Confidence Interval | adjusted score change | Day 0 to Day 84 |
|
The adverse event data was collected during the weeks 0-24.
Patients could self-report Adverse Events using a open-ended repeatedly prompted within-intervention questionnaire, a Jira questionnaire available in intervention main menu, email, and phone calls to clinical subject coordinators.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | MEL-T01 | MEL-T01 is a game-based digital-therapeutics (DTx) medical software device that implements personalised cognitive training to alleviate MDD symptoms and improve cognitive performance in MDD subjects. MEL-T01: A 12 week intervention with MEL-T01. |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Frustration | Product Issues | Non-systematic Assessment |
Not reaching the intended number (n = 133) of completer subjects in MEL-T01 (n = 99) and MEL-S01 (n = 96) arms.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Prof. J. Matias Palva | Aalto University | +358401547779 | matias.palva@aalto.fi |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Feb 26, 2024 | Oct 10, 2025 | Prot_SAP_000.pdf |
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| ID | Term |
|---|---|
| D003865 | Depressive Disorder, Major |
| D003863 | Depression |
| ID | Term |
|---|---|
| D003866 | Depressive Disorder |
| D019964 | Mood Disorders |
| D001523 | Mental Disorders |
| D001526 | Behavioral Symptoms |
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The effectiveness of MEL-T01 and comparator MEL-S01 are studied. Their effectiveness is compared to a treatment-as-usual (TAU) group who also receive the intervention after a 12 week waiting period.
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The research design is randomized and double-blinded. Subject randomization in study arms as well as treatment is automatized.
| MEL-S01 | Device | A 12 week intervention with MEL-S01. |
|
| Day 0 to Day 84 |
| RRS (Short Version) Total Change From Baseline to Posttreatment | Ruminative Response Scale (RRS), short version, is an eight item self-report questionnaire that uses a four point Likert-scale. This leads to a total score between 8 and 64 where higher values indicate higher depressive brooding. For each of the three study arms, the change in total RRS scores between before the intervention compared and after the 12 week intervention are measured. Then, the average change scores in each of the three groups are compared with each other. | Day 0 to Day 84 |
| GAD-7 Total Change From Baseline to Posttreatment | The general anxiety disorder scale (GAD-7) is a seven-item self-report questionnaire that uses a 4-point scale (between 0 and 3) to evaluate the degree of anxiety symptoms. The questionnaire provides a total between 0 and 21: the higher the total score, the more severe the anxiety. For each of the three study arms, the change in total GAD-7 scores between before the intervention and after the 12 week intervention is measured. Then, the average change scores in each of the three groups are compared with each other. | Day 0 to Day 84 |
| SDS Total Change From Baseline to Posttreatment | The Sheehan disability scale (SDS) is a self-administered three item questionnaire using a 11-point scale (between 0 and 10). The scale is used to measure functional impairment. The scale provides a total score between 0 and 30: the higher the score, the higher the functional impairment. In addition, the scale measures "the number of days lost to symptoms" and "the number of days unproductive due to the symptoms". For each of the three study arms, the change in total SDS scores between before the intervention and after the 12 week intervention is measured. Then, the average change scores in each of the three groups are compared with each other. | Day 0 to Day 84 |
| PVSS Total Change From Baseline to Posttreatment | The positive valence systems scale (PVSS) is a 21-item self-report questionnaire using a scale from 1 to 9. This leads to a total score between 21 and 189 where a lower total score indicates higher anhedonia. For each of the three study arms, the change in total PVSS scores between before the intervention and after the 12 week intervention is measured. Then, the average change scores in each of the three groups are compared with each other. | Day 0 to Day 84 |
| WHO-5 Total Change From Baseline to Posttreatment | The well-being index (WHO-5) is a five item self-report questionnaire using a scale from 0 to 5. This leads to a total score is between 0 and 25: higher scores indicate higher subjective well-being. For each of the three study arms, the change in total WHO-5 scores between before the intervention and after the 12 week intervention is measured. Then, the average change scores in each of the three groups are compared with each other. | Day 0 to Day 84 |
| Correlation Between PHQ-9 Total Change and Playing Time in Group MEL-T01 | The patient health questionnaire (PHQ-9, Kroenke et al., 2001) is a self-report measure of major depressive disorder. The PHQ-9 scores each of the nine DSM-IV criteria for MDD from "0" (not at all) to "3" (nearly every day), providing a 0-27 severity score of depression. The higher the total score the more severe the depression. For the treatment MEL-T01 group, the change scores in the total PHQ-9 score between before the intervention and after the 12 week intervention is measured. Then, the correlation between the change score and the minutes played during the intervention is calculated. This leads to a correlation score that evaluates whether a higher symptom change is associated with higher playing time. | Day 0 to Day 84 |
| Correlation Between PHQ-9 Total Change and Playing Time in Group MEL-S01 | The patient health questionnaire (PHQ-9, Kroenke et al., 2001) is a self-report measure of major depressive disorder. The PHQ-9 scores each of the nine DSM-IV criteria for MDD from "0" (not at all) to "3" (nearly every day), providing a 0-27 severity score of depression. The higher the total score the more severe the depression. For the active comparator MEL-S01 group, the change scores in the total PHQ-9 score between before the intervention and after the 12 week intervention is measured. Then, the correlation between the change score and the minutes played during the intervention is calculated. This leads to a correlation score that evaluates whether a higher symptom change is associated with higher playing time. | Day 0 to Day 84 |
| Correlation Between PHQ-9 Total Change and IEQ in Group MEL-T01 | The immersive experiences questionnaire (IEQ, Jennett et al., 2008) is a self-report questionnaire that measures the subjective experience of being immersed while playing a video game. It has 31 questions on a scale of 1-7. This creates a total score between 31 and 217: the higher totals indicate higher immersion. In addition, there is one question - "How immersed did you feel?" - on a scale of 1-10. For the treatment MEL-T01 group, we measure the correlation between 1) the change in the total PHQ-9 score between before the intervention and after the 12 week intervention and 2) the total IEQ score (excluding the one additional questionnaire) as measured after the 12 week intervention. This leads to a correlation score that evaluates whether a higher symptom change is associated with higher immersion in the game. | Day 0 to Day 84 |
| Correlation Between PHQ-9 Total Change and IEQ in Group MEL-S01 | The immersive experiences questionnaire (IEQ, Jennett et al., 2008) is a self-report questionnaire that measures the subjective experience of being immersed while playing a video game. It has 31 questions on a scale of 1-7. This creates a total score between 31 and 217: the higher totals indicate higher immersion. In addition, there is one question - "How immersed did you feel?" - on a scale of 1-10. For the treatment MEL-S01 group, we measure the correlation between 1) the change in the total PHQ-9 score between before the intervention and after the 12 week intervention and 2) the total IEQ score (excluding the one additional questionnaire) as measured after the 12 week intervention. This leads to a correlation score that evaluates whether a higher symptom change is associated with higher immersion in the game. | Day 0 to Day 84 |
| Day 0 to Day 84 |
| Espoo |
| Uusimaa |
| 02150 |
| Finland |
| Aalto University, Department of Neuroscience and Biomedical Engineering | Espoo | Uusimaa | 02150 | Finland |
| Helsinki University Hospital, Psychiatry | Helsinki | Uusimaa | 00014 | Finland |
| Helsinki University Hospital BioMag laboratory | Helsinki | Uusimaa | 00029 | Finland |
| University of Helsinki Neuroscience Center (MEG, MRI) | Helsinki | Uusimaa | Finland |
MEL-S01 is an active comparator similar to MEL-T01 but without personalized cognitive training elements. MEL-S01: A 12 week intervention with MEL-S01. |
| BG002 | TAU (Treatment-As-Usual) | Treatment-as-usual in healthcare. |
| BG003 | Total | Total of all reporting groups |
| years |
|
| Sex/Gender, Customized | Count of Participants | Participants |
|
| Race and Ethnicity Not Collected | Race and Ethnicity were not collected from any participant. | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| PHQ-9 | The patient health questionnaire (PHQ-9, Kroenke et al., 2001) is a self-report measure of major depressive disorder. The PHQ-9 scores each of the nine DSM-IV criteria for MDD from "0" (not at all) to "3" (nearly every day), providing a 0-27 severity score of depression. The higher the total score the more severe the depression. | Mean | Standard Deviation | units on a scale |
|
MEL-T01 is a game-based digital-therapeutics (DTx) medical software device that implements personalised cognitive training to alleviate MDD symptoms and improve cognitive performance in MDD subjects. MEL-T01: A 12 week intervention with MEL-T01 as adjunct to TAU. TAU: Treatment As Usual in healthcare. |
| OG001 | Treatment As Usual (TAU) | Treatment As Usual in healthcare for 12 weeks. This group combines both "First TAU, then MEL-T01" and "First TAU, then MEL-S01". |
|
|
|
| Primary | PHQ-9 Total Change From Baseline to Posttreatment: Active Comparator Group vs. Treatment as Usual Group | The patient health questionnaire (PHQ-9, Kroenke et al., 2001) is a self-report measure of major depressive disorder. The PHQ-9 scores each of the nine DSM-IV criteria for MDD from "0" (not at all) to "3" (nearly every day), providing a 0-27 severity score of depression. The higher the total score the more severe the depression. The change in the PHQ-9 total score between before the 12 week intervention and after the intervention is measured. The change score of MEL-S01 group is compared with the change score of the treatment-as-usual (TAU) group. | Per protocol completer cohort. Analyses were restricted to weeks 0-12; TAU participants were pooled as all received identical treatment during this period, regardless of later allocation. | Posted | Least Squares Mean | 90% Confidence Interval | adjusted score change | Day 0 to Day 84 |
|
|
|
|
| Primary | PHQ-9 Total Change From Baseline to Posttreatment: Experimental Group vs. Active Comparator Group | The patient health questionnaire (PHQ-9, Kroenke et al., 2001) is a self-report measure of major depressive disorder. The PHQ-9 scores each of the nine DSM-IV criteria for MDD from "0" (not at all) to "3" (nearly every day), providing a 0-27 severity score of depression. The higher the total score the more severe the depression. The change in the PHQ-9 total score between before the 12 week intervention and after the intervention is measured. The change score of MEL-T01 group is compared with the change score in the MEL-S01 group. | Per protocol completer cohort. Analyses were restricted to weeks 0-12. | Posted | Least Squares Mean | 90% Confidence Interval | adjusted score change | Day 0 to Day 84 |
|
|
|
|
| Secondary | QIDS Total Change From Baseline to Posttreatment | The quick inventory of depressive symptomatology (QIDS-SR16) is a self-report measure comprising of 16 questions on a scale of 0-3 which assess the severity of depressive symptoms. The inventory provides a total score between 0 and 48: the higher the total score the more severe the depression. For each of the three study arms, the change in total QIDS-SR16 scores between before the intervention and after the 12 week intervention is measured. Then, the average change scores in each of the three groups are compared with each other. | Per protocol completer cohort. Analyses were restricted to weeks 0-12; TAU participants were pooled as all received identical treatment during this period, regardless of later allocation. | Posted | Least Squares Mean | 90% Confidence Interval | adjusted score change | Day 0 to Day 84 |
|
|
|
|
| Secondary | RRS (Short Version) Total Change From Baseline to Posttreatment | Ruminative Response Scale (RRS), short version, is an eight item self-report questionnaire that uses a four point Likert-scale. This leads to a total score between 8 and 64 where higher values indicate higher depressive brooding. For each of the three study arms, the change in total RRS scores between before the intervention compared and after the 12 week intervention are measured. Then, the average change scores in each of the three groups are compared with each other. | Per protocol completer cohort. Analyses were restricted to weeks 0-12; TAU participants were pooled as all received identical treatment during this period, regardless of later allocation. | Posted | Least Squares Mean | 90% Confidence Interval | adjusted score change | Day 0 to Day 84 |
|
|
|
|
| Secondary | GAD-7 Total Change From Baseline to Posttreatment | The general anxiety disorder scale (GAD-7) is a seven-item self-report questionnaire that uses a 4-point scale (between 0 and 3) to evaluate the degree of anxiety symptoms. The questionnaire provides a total between 0 and 21: the higher the total score, the more severe the anxiety. For each of the three study arms, the change in total GAD-7 scores between before the intervention and after the 12 week intervention is measured. Then, the average change scores in each of the three groups are compared with each other. | Per protocol completer cohort. Analyses were restricted to weeks 0-12; TAU participants were pooled as all received identical treatment during this period, regardless of later allocation. | Posted | Least Squares Mean | 90% Confidence Interval | adjusted score change | Day 0 to Day 84 |
|
|
|
|
| Secondary | SDS Total Change From Baseline to Posttreatment | The Sheehan disability scale (SDS) is a self-administered three item questionnaire using a 11-point scale (between 0 and 10). The scale is used to measure functional impairment. The scale provides a total score between 0 and 30: the higher the score, the higher the functional impairment. In addition, the scale measures "the number of days lost to symptoms" and "the number of days unproductive due to the symptoms". For each of the three study arms, the change in total SDS scores between before the intervention and after the 12 week intervention is measured. Then, the average change scores in each of the three groups are compared with each other. | Per protocol completer cohort. Analyses were restricted to weeks 0-12; TAU participants were pooled as all received identical treatment during this period, regardless of later allocation. | Posted | Least Squares Mean | 90% Confidence Interval | adjusted score change | Day 0 to Day 84 |
|
|
|
|
| Secondary | PVSS Total Change From Baseline to Posttreatment | The positive valence systems scale (PVSS) is a 21-item self-report questionnaire using a scale from 1 to 9. This leads to a total score between 21 and 189 where a lower total score indicates higher anhedonia. For each of the three study arms, the change in total PVSS scores between before the intervention and after the 12 week intervention is measured. Then, the average change scores in each of the three groups are compared with each other. | Per protocol completer cohort. Analyses were restricted to weeks 0-12; TAU participants were pooled as all received identical treatment during this period, regardless of later allocation. | Posted | Least Squares Mean | 90% Confidence Interval | adjusted score change | Day 0 to Day 84 |
|
|
|
|
| Secondary | WHO-5 Total Change From Baseline to Posttreatment | The well-being index (WHO-5) is a five item self-report questionnaire using a scale from 0 to 5. This leads to a total score is between 0 and 25: higher scores indicate higher subjective well-being. For each of the three study arms, the change in total WHO-5 scores between before the intervention and after the 12 week intervention is measured. Then, the average change scores in each of the three groups are compared with each other. | Per protocol completer cohort. Analyses were restricted to weeks 0-12; TAU participants were pooled as all received identical treatment during this period, regardless of later allocation. | Posted | Least Squares Mean | 90% Confidence Interval | adjusted score change | Day 0 to Day 84 |
|
|
|
|
| Secondary | Correlation Between PHQ-9 Total Change and Playing Time in Group MEL-T01 | The patient health questionnaire (PHQ-9, Kroenke et al., 2001) is a self-report measure of major depressive disorder. The PHQ-9 scores each of the nine DSM-IV criteria for MDD from "0" (not at all) to "3" (nearly every day), providing a 0-27 severity score of depression. The higher the total score the more severe the depression. For the treatment MEL-T01 group, the change scores in the total PHQ-9 score between before the intervention and after the 12 week intervention is measured. Then, the correlation between the change score and the minutes played during the intervention is calculated. This leads to a correlation score that evaluates whether a higher symptom change is associated with higher playing time. | Intention-to-treat cohort. | Posted | Number | 95% Confidence Interval | fixed effect coefficient | Day 0 to Day 84 |
|
|
|
|
| Secondary | Correlation Between PHQ-9 Total Change and Playing Time in Group MEL-S01 | The patient health questionnaire (PHQ-9, Kroenke et al., 2001) is a self-report measure of major depressive disorder. The PHQ-9 scores each of the nine DSM-IV criteria for MDD from "0" (not at all) to "3" (nearly every day), providing a 0-27 severity score of depression. The higher the total score the more severe the depression. For the active comparator MEL-S01 group, the change scores in the total PHQ-9 score between before the intervention and after the 12 week intervention is measured. Then, the correlation between the change score and the minutes played during the intervention is calculated. This leads to a correlation score that evaluates whether a higher symptom change is associated with higher playing time. | Intention-to-treat cohort. | Posted | Number | 95% Confidence Interval | fixed effect coefficient | Day 0 to Day 84 |
|
|
|
|
| Secondary | Correlation Between PHQ-9 Total Change and IEQ in Group MEL-T01 | The immersive experiences questionnaire (IEQ, Jennett et al., 2008) is a self-report questionnaire that measures the subjective experience of being immersed while playing a video game. It has 31 questions on a scale of 1-7. This creates a total score between 31 and 217: the higher totals indicate higher immersion. In addition, there is one question - "How immersed did you feel?" - on a scale of 1-10. For the treatment MEL-T01 group, we measure the correlation between 1) the change in the total PHQ-9 score between before the intervention and after the 12 week intervention and 2) the total IEQ score (excluding the one additional questionnaire) as measured after the 12 week intervention. This leads to a correlation score that evaluates whether a higher symptom change is associated with higher immersion in the game. | Intention-to-treat cohort. | Posted | Number | 95% Confidence Interval | fixed effect coefficient | Day 0 to Day 84 |
|
|
|
|
| Secondary | Correlation Between PHQ-9 Total Change and IEQ in Group MEL-S01 | The immersive experiences questionnaire (IEQ, Jennett et al., 2008) is a self-report questionnaire that measures the subjective experience of being immersed while playing a video game. It has 31 questions on a scale of 1-7. This creates a total score between 31 and 217: the higher totals indicate higher immersion. In addition, there is one question - "How immersed did you feel?" - on a scale of 1-10. For the treatment MEL-S01 group, we measure the correlation between 1) the change in the total PHQ-9 score between before the intervention and after the 12 week intervention and 2) the total IEQ score (excluding the one additional questionnaire) as measured after the 12 week intervention. This leads to a correlation score that evaluates whether a higher symptom change is associated with higher immersion in the game. | Intention-to-treat cohort. | Posted | Number | 95% Confidence Interval | fixed effect coefficient | Day 0 to Day 84 |
|
|
|
|
| Other Pre-specified | GAS Total Change From Baseline to Posttreatment | The game addiction scale (GAS, Lemmens et al., 2009) is a self-report 7-item questionnaire using a 1-5 scale which measures game addiction. This provides a total between 7 and 35: the higher the scores indicate higher addiction. For each of the three study arms, the change in total GAS scores between before the intervention and after the 12 week intervention is measured. Then, the average change scores in each of the three groups are compared with each other. | Per protocol completer cohort. Analyses were restricted to weeks 0-12; TAU participants were pooled as all received identical treatment during this period, regardless of later allocation. | Posted | Least Squares Mean | 90% Confidence Interval | adjusted score change | Day 0 to Day 84 |
|
|
|
|
| 0 |
| 337 |
| 0 |
| 337 |
| 52 |
| 337 |
| EG001 | MEL-S01 | MEL-S01 is an active comparator similar to MEL-T01 but without personalized cognitive training elements. MEL-S01: A 12 week intervention with MEL-S01. | 0 | 347 | 0 | 347 | 55 | 347 |
| EG002 | TAU (Treatment-As-Usual; First TAU, Then MEL-T01) | Treatment-as-usual in healthcare for 12 weeks. Then, the participant is given acess to MEL-T01 for 12 weeks. | 0 | 153 | 0 | 153 | 16 | 153 |
| EG003 | TAU (Treatment-As-Usual; First TAU, Then MEL-S01) | Treatment-as-usual in healthcare for 12 weeks. Then, the participant is given acess to MEL-S01 for 12 weeks. | 0 | 164 | 0 | 164 | 24 | 164 |
| Stress | Product Issues | Non-systematic Assessment |
|
| Anxiety | Psychiatric disorders | Non-systematic Assessment |
|
| Nausea | General disorders | Non-systematic Assessment |
|
| Headache | General disorders | Non-systematic Assessment |
|
| Arm and neck pain | General disorders | Non-systematic Assessment |
|
| PTSD exacerbates | Psychiatric disorders | Non-systematic Assessment |
|
| Audiovisual discomfort | Product Issues | Non-systematic Assessment |
|
| Nightmares | Psychiatric disorders | Non-systematic Assessment |
|
Not provided
Not provided
| D001519 |
| Behavior |
| Title | Measurements |
|---|---|
|
| Title | Measurements |
|---|---|
|
| Mixed Models Analysis |
Robust linear mixture model (rlmer). DoF with Satterthweite. Robust Wald-type tests for p-values. |
| 0.00084 |
Alpha level 0.05. Holm-Bonferroni correction applied across comparisons. |
| adjusted mean difference |
| -0.598 |
| 2-Sided |
| 90 |
| -0.909 |
| -0.287 |
| Superiority |
| Mixed Models Analysis | Robust linear mixture model (rlmer). DoF with Satterthweite. Robust Wald-type tests for p-values. | <0.0000001 | Alpha level 0.05. Holm-Bonferroni correction applied across comparisons. | adjusted mean difference | -1.121 | 2-Sided | 90 | -1.429 | -0.814 | Superiority |
| Mixed Models Analysis |
Robust linear mixture model (rlmer). DoF with Satterthweite. Robust Wald-type tests for p-values. |
| 0.879 |
Alpha level 0.05. Holm-Bonferroni correction applied across comparisons. |
| adjusted mean difference |
| 0.233 |
| 2-Sided |
| 90 |
| -0.094 |
| 0.560 |
| Superiority |
| Mixed Models Analysis | Robust linear mixture model (rlmer). DoF with Satterthweite. Robust Wald-type tests for p-values. | 0.194 | Alpha level 0.05. Holm-Bonferroni correction applied across comparisons. | adjusted mean difference | -0.170 | 2-Sided | 90 | -0.492 | 0.153 | Superiority |
| Mixed Models Analysis |
Robust linear mixture model (rlmer). DoF with Satterthweite. Robust Wald-type tests for p-values. |
| 0.059 |
Alpha level 0.05. Holm-Bonferroni correction applied across comparisons. |
| adjusted mean difference |
| -0.371 |
| 2-Sided |
| 90 |
| -0.761 |
| 0.019 |
| Superiority |
| Mixed Models Analysis | Robust linear mixture model (rlmer). DoF with Satterthweite. Robust Wald-type tests for p-values. | 0.00021 | Alpha level 0.05. Holm-Bonferroni correction applied across comparisons. | adjusted mean difference | -0.832 | 2-Sided | 90 | -1.218 | -0.447 | Superiority |
| Mixed Models Analysis |
Robust linear mixture model (rlmer). DoF with Satterthweite. Robust Wald-type tests for p-values. |
| 0.014 |
Alpha level 0.05. Holm-Bonferroni correction applied across comparisons. |
| adjusted mean difference |
| -0.769 |
| 2-Sided |
| 89 |
| -1.342 |
| -0.196 |
| Superiority |
| Mixed Models Analysis | Robust linear mixture model (rlmer). DoF with Satterthweite. Robust Wald-type tests for p-values. | 0.000031 | Alpha level 0.05. Holm-Bonferroni correction applied across comparisons. | adjusted mean difference | -1.391 | 2-Sided | 90 | -1.958 | -0.825 | Superiority |
| Mixed Models Analysis |
Robust linear mixture model (rlmer). DoF with Satterthweite. Robust Wald-type tests for p-values. |
| 0.00000011 |
Alpha level 0.05. Holm-Bonferroni correction applied across comparisons. |
| adjusted mean difference |
| 7.378 |
| 2-Sided |
| 90 |
| 5.070 |
| 9.687 |
| Superiority |
| Mixed Models Analysis | Robust linear mixture model (rlmer). DoF with Satterthweite. Robust Wald-type tests for p-values. | 0.00000041 | Alpha level 0.05. Holm-Bonferroni correction applied across comparisons. | adjusted mean difference | 6.950 | 2-Sided | 90 | 4.661 | 9.238 | Superiority |
| Mixed Models Analysis |
Robust linear mixture model (rlmer). DoF with Satterthweite. Robust Wald-type tests for p-values. |
| <0.0000001 |
Alpha level 0.05. Holm-Bonferroni correction applied across comparisons. |
| adjusted mean difference |
| 1.047 |
| 2-Sided |
| 90 |
| 0.760 |
| 1.335 |
| Superiority |
| Mixed Models Analysis | Robust linear mixture model (rlmer). DoF with Satterthweite. Robust Wald-type tests for p-values. | <0.0000001 | Alpha level 0.05. Holm-Bonferroni correction applied across comparisons. | adjusted mean difference | 0.992 | 2-Sided | 90 | 0.707 | 1.276 | Superiority |
|
| Mixed Models Analysis |
Robust linear mixture model (rlmer). DoF with Satterthweite. Robust Wald-type tests for p-values. |
| 0.132 |
Two-tailed, alpha level 0.025. Holm-Bonferroni correction applied across comparisons. |
| adjusted mean difference |
| 0.137 |
| 2-Sided |
| 95 |
| -0.012 |
| 0.286 |
| Equivalence |
Testing whether the GAS change in the two groups is equal. |
| Mixed Models Analysis | Robust linear mixture model (rlmer). DoF with Satterthweite. Robust Wald-type tests for p-values. | 0.176 | Two-tailed, alpha level 0.025. Holm-Bonferroni correction applied across comparisons. | adjusted mean difference | -0.121 | 2-Sided | 95 | -0.269 | 0.026 | Equivalence | Testing whether the GAS change in the two groups is equal. |