Quality of Life Clinical Trial
Official title:
Effects of Social Media-based Electronic Bibliotherapy on Improving the Well-being of Informal Caregivers of People With Dementia
NCT number | NCT06327022 |
Other study ID # | P0038444 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | July 1, 2022 |
Est. completion date | December 31, 2023 |
Verified date | February 2024 |
Source | The Hong Kong Polytechnic University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study aims to assess the efficacy of social media-based electronic bibliotherapy in improving the well-being of informal caregivers of people with dementia compared to a control group.
Status | Completed |
Enrollment | 60 |
Est. completion date | December 31, 2023 |
Est. primary completion date | December 31, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - caregivers providing regular care to individuals with mild to moderately severe dementia (Global Deterioration Scale=4~6 of any type), requiring at least five hours per week for a minimum duration of six months; - aged 18 or above; - not receiving payment for caregiving services rendered; - assisting with at least one daily activity of the care recipient; - possessing reading ability; - utilized social media platforms such as WhatsApp, Facebook, Twitter, Instagram, and WeChat for over six months. Exclusion Criteria: - caregivers with unstable physical or mental conditions; - caregivers unable to communicate logically; - involvement in another interventional study |
Country | Name | City | State |
---|---|---|---|
Hong Kong | The Hong Kong Polytechnic University | Kowloon |
Lead Sponsor | Collaborator |
---|---|
The Hong Kong Polytechnic University |
Hong Kong,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in mental health | Mental health will be measured with the Depression Anxiety Stress Scale-21. It is a 4-point Likert scale consisting of 21 items that measure levels ofdepression, anxiety, and stress in participants. Higher scores indicategreater severity of mental health problems. | Pre-intervention, post-intervention (i.e., within one week after completing the intervention) | |
Secondary | Changes in health related quality of life | The health-related quality of life will be assessed using the 12-item Short Form Survey. It comprises two domains, namely the physical component summary and the mental component summary. Higher scores indicate better health-related quality of life. | Pre-intervention, post-intervention (i.e., within one week after completing the intervention) | |
Secondary | Changes in caregiving appraisal | Caregiving appraisal will be assessed using the Caregiving Appraisal Scale. It is a 26-item Likert scale ranging from 1 (strongly disagree) to 5 (strongly agree). Higher scores on this scale indicate more positive caregiving appraisal. | Pre-intervention, post-intervention (i.e., within one week after completing the intervention) | |
Secondary | Changes in psychological wellbeing | The psychological well-being will be assessed using the shorter Chinese version of Ryff's psychological well-being scale. This scale is a Likert 6-point scale (1=strongly disagree, 6=strongly agree) comprising 18 items. Higher scores indicate greater levels of psychological well-being. | Pre-intervention, post-intervention (i.e., within one week after completing the intervention) |
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