Dementia Clinical Trial
Official title:
Design and Pilot-test of an Innovative Mobile-based Intervention to Promote Mental Health of Informal Dementia Caregivers Through User-Centered Design
Informal caregivers of persons with dementia (PWD) usually experience elevated levels of caregiving burden and potential depression. This project aims to develop and pilot-test a mobile app intervention for informal caregivers of PWD in Singapore. The project will have three phases in total including 1) phase 1 - to develop the app prototype and collect feedback from caregivers via focused group discussions. 2) a pilot RCT with 60 participants in total - 30 will be required to use the app for one month while another 30 will be on a waiting list for one month. and 3) in-depth interviews to seek users' feedback on the app for its future improvements. We hypothesize that the mobile app designed through a user-centered process would lead to high acceptance and high user engagement among local dementia caregivers. The 1-month intervention using the app developed subsequently would lower the reported depressive symptoms among local dementia caregiver. It will also improve their knowledge of dementia, caregiving efficacy, positive coping strategy, perceived positive aspects of caregiver and social support, and their mental well-being; and reduce their caregiving burden, and level of anxiety, compared to the control group.
Status | Recruiting |
Enrollment | 60 |
Est. completion date | June 2024 |
Est. primary completion date | March 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 21 Years and older |
Eligibility | Inclusion Criteria: 1. aged 21 or above; 2. Singapore citizen or permanent resident; 3. primary caregiver who is currently taking care of a PWD; 4. scores 4 and above using the 4-item screening version Zarit Burden Interview; 5. has sufficient skills in using mobile apps; 6. able to read, write, and speak in English Exclusion Criteria: 1. Caregivers who are pregnant 2. caregivers with vision and hearing problems |
Country | Name | City | State |
---|---|---|---|
Singapore | Clinic B, Institute of Mental Health | Singapore |
Lead Sponsor | Collaborator |
---|---|
Institute of Mental Health, Singapore | National Healthcare Group, Singapore |
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* Note: There are 12 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Baseline depressive symptom | Centre for Epidemiological Study Scale (0-60), with a higher score indicating a more severe depressive symptom | baseline - before the intervention | |
Primary | Post-intervention depressive symptom | Centre for Epidemiological Study Scale (0-60), with a higher score indicating a more severe depressive symptom | within 2 weeks after the intervention | |
Secondary | Baseline knowledge of dementia | Dementia Knowledge Assessment Scale (0-54), with higher score indicating better knowledge on dementia | baseline - before the intervention | |
Secondary | Post intervention knowledge of dementia | Dementia Knowledge Assessment Scale (0-54), with higher score indicating better knowledge on dementia | within 2 weeks after the intervention | |
Secondary | Baseline caregiving self-efficacy | Revised Scale for Caregiving Self-efficacy (0-100), with higher score indicating more confidence in caregiving | baseline - before the intervention | |
Secondary | Post intervention caregiving self-efficacy | Revised Scale for Caregiving Self-efficacy (0-100), with higher score indicating more confidence in caregiving | within 2 weeks after the intervention | |
Secondary | Baseline coping strategy | brief Coping Orientation to Problems Experienced inventory - it has a total of 14 subscales, for each subscale higher score indicating more frequent usage of that specific coping strategy | baseline - before the intervention | |
Secondary | Post intervention coping strategy | brief Coping Orientation to Problems Experienced inventory - it has a total of 14 subscales, for each subscale higher score indicating more frequent usage of that specific coping strategy | within 2 weeks after the intervention | |
Secondary | Baseline positive aspects of caregiving | Positive Aspects of Caregiving Scale (9-45) - with a higher score indicates a more positive caregiving experience | baseline - before the intervention | |
Secondary | Post intervention positive aspects of caregiving | Positive Aspects of Caregiving Scale (9-45) - with a higher score indicates a more positive caregiving experience | within 2 weeks after the intervention | |
Secondary | Baseline caregiver burden | Zarit burden interview (0-88) - with a higher score indicating higher perceived caregiving burden | baseline - before the intervention | |
Secondary | Post intervention caregiver burden | Zarit burden interview (0-88) - with a higher score indicating higher perceived caregiving burden | within 2 weeks after the intervention | |
Secondary | Baseline anxiety level | Generalized Anxiety Disorder 7-item scale (0-21) - with a higher score indicating higher anxiety level | baseline - before the intervention | |
Secondary | Post intervention anxiety level | Generalized Anxiety Disorder 7-item scale (0-21) - with a higher score indicating higher anxiety level | within 2 weeks after the intervention | |
Secondary | Baseline mental well-being | Short Positive Mental Health instrument (1-6) - with a higher score indicating higher positive mental health | baseline - before the intervention | |
Secondary | Post intervention mental well-being | Short Positive Mental Health instrument (1-6) - with a higher score indicating higher positive mental health | within 2 weeks after the intervention |
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