Not provided
| ID | Type | Description | Link |
|---|---|---|---|
| 2018-87 | Other Identifier | FujianMU |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Based on the changing law of cognitive function, combined with the behavior change wheel theory and the health behavior process orientation model, we constructed a mobile health management program for geriatric depression. The aim is to explore the effect of this intervention program on the health behavior of elderly patients with depression; and to verify the effect of the intervention program on improving the primary outcome and other secondary outcomes of elderly patients with depression, with a view to providing a scientific basis for the management of depression in the elderly and promoting the optimization of personalized intervention strategies.
Based on the changing law of cognitive function, combined with the behavior change wheel theory and the health behavior process orientation model, we constructed a mobile health management program for geriatric depression. The aim is to explore the effect of this intervention program on the health behavior of elderly patients with depression; and to verify the effect of the intervention program on improving the primary outcome and other secondary outcomes of elderly patients with depression, with a view to providing a scientific basis for the management of depression in the elderly and promoting the optimization of personalized intervention strategies.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Intervention Group (Mobile Health Management Intervention) | Experimental | Participants in this group will receive a mobile health management intervention over a period of 12 weeks. This intervention includes the use of a mobile application designed for health management, psychological support, and monitoring，et al, with the aim of improving the mental health status of elderly patients with depression. |
|
| Control Group (Standard Care) | No Intervention | Participants in this group will receive standard care during the same 12-week period. This includes routine medical services and psychological support, but does not involve any specific mobile health intervention. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Intervention Group (Mobile Health Management Intervention) | Device | Participants in this group will receive a mobile health management intervention over a period of 12 weeks. This intervention includes the use of a mobile application designed for health management, psychological support, and monitoring,et al， with the aim of improving the mental health status of elderly patients with depression. |
| Measure | Description | Time Frame |
|---|---|---|
| cognitive function | Using Montreal Cognitive Assessment（ MoCA） to assess patients' cognitive function | From baseline (T0) to 6 weeks post-intervention (T1) and 12 weeks post-intervention (T2) |
| Measure | Description | Time Frame |
|---|---|---|
| depressive symptoms | sing the Geriatric Depression Scale (GDS-15) to assess patients' depressive symptoms. | From baseline (T0) to 6 weeks post-intervention (T1) and 12 weeks post-intervention (T2) |
| Behavioral Inhibition /Behavioral Activation |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Fujian Medial University | Fuzhou | Fujian | 350100 | China |
2025.7.1
Not provided
Not provided
Not provided
Not provided
This study employs a parallel assignment design where participants are randomly assigned to either the experimental group receiving Mobile Health Management Intervention or the control group receiving a standard treatment. The study is single-blind, meaning participants are unaware of which group they belong to, thus minimizing potential bias. Data will be collected at regular intervals to evaluate the efficacy and safety of the intervention.
Not provided
Not provided
Not provided
|
Using the Behavioral Inhibition System/Behavioral Activation System Scale (BIS/BAS) to assess patients' behavior.
| From baseline (T0) to 6 weeks post-intervention (T1) and 12 weeks post-intervention (T2) |
| patients' quality of life | Using the WHO QOL-BREF to assess patients' quality of life. | From baseline (T0) to 6 weeks post-intervention (T1) and 12 weeks post-intervention (T2) |
| sleep quality | Using the Pittsburgh Sleep Quality Index (PSQI) to assess patients' sleep quality. | From baseline (T0) to 6 weeks post-intervention (T1) and 12 weeks post-intervention (T2) |
| psychological needs | Using the Basic Psychological Needs Scale (BPNS) to assess patients' psychological needs. | From baseline (T0) to 6 weeks post-intervention (T1) and 12 weeks post-intervention (T2) |