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| Name | Class |
|---|---|
| University of Groningen | OTHER |
| Dutch Cancer Society | OTHER |
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The purpose of this study is to determine whether mindfulness-based cognitive therapy (MBCT) and cognitive behavioral therapy (CBT) are effective in reducing depressive symptoms in patients after cancer
Cancer patients are prone to develop depressive symptoms, even after curative treatment. Conventional therapies such as cognitive behavioral therapy (CBT) and mindfulness-based cognitive therapy (MBCT) are frequently used for reducing these depressive symptoms in patients with medical conditions. However, until now evidence from proper designed randomized controlled trials regarding the effectiveness of both interventions in cancer survivors, is lacking. Therefore, our longitudinal study aims to investigate the effectiveness of CBT and MBCT in reducing depressive symptoms in cancer survivors. In addition, potential moderators and mediators of each intervention will be explored.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| MBCT | Experimental | Mindfulness-Based Cognitive Therapy |
|
| CBT | Experimental | Cognitive Behavioral Therapy |
|
| TAU | No Intervention | Treatment as usual |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Mindfulness-Based Cognitive Therapy (MBCT) | Behavioral | The intervention consists of 8 weekly individual sessions of MBCT. Each session will be administered individually and will last 60 minutes |
| Measure | Description | Time Frame |
|---|---|---|
| Change in severity of depressive symptoms | Severity of depressive symptoms will be assessed with the Beck Depression Inventory-II (BDI-II) | pre-treatment (baseline) to post-treatment (approximately 3 months after baseline) and 3- and 9-month follow-up |
| Measure | Description | Time Frame |
|---|---|---|
| Change in generalized anxiety | Generalized anxiety is measured by the Generalised Anxiety Disorder Assessment (GAD 7) | pre-treatment (baseline) to post-treatment (approximately 3 months after baseline) and 3- and 9-month follow-up |
| Change in well-being |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Annika Tovote, Dr. | Contact | 0031(0)503632955 | k.a.tovote@umcg.nl |
| Name | Affiliation | Role |
|---|---|---|
| Maya Schroevers, Dr. | University Medical Center Groningen | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| UMCG | Recruiting | Groningen | Provincie Groningen | Netherlands |
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| ID | Term |
|---|---|
| D003863 | Depression |
| D009369 | Neoplasms |
| ID | Term |
|---|---|
| D001526 | Behavioral Symptoms |
| D001519 | Behavior |
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| ID | Term |
|---|---|
| D000099025 | Mindfulness-Based Cognitive Therapy |
| D015928 | Cognitive Behavioral Therapy |
| ID | Term |
|---|---|
| D064866 | Mindfulness |
| D001521 | Behavior Therapy |
| D011613 | Psychotherapy |
| D004191 | Behavioral Disciplines and Activities |
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| Cognitive Behavioral Therapy (CBT) | Behavioral | The intervention consists of 8 weekly individual sessions of CBT. Each session will be administered individually and will last 60 minutes. |
|
Well-being is measured by the WHO Well-being Index (WHO-5) |
| pre-treatment (baseline) to post-treatment (approximately 3 months after baseline) and 3- and 9-month follow-up |
| Change in fear of recurrence | Fear of recurrence will be measured by Concerns About Recurrence Scale (CARS) | pre-treatment (baseline) to post-treatment (approximately 3 months after baseline) and 3- and 9-month follow-up |
| Change in fatigue | Fatigue is measured by the subsequent scale of the Multidimensional Fatigue Inventory (MFI-20) | pre-treatment (baseline) to post-treatment (approximately 3 months after baseline) and 3- and 9-month follow-up |