Enhancing Life Quality in Community-Dwelling Older Omanis by Telling Their Life Story
1 other identifier
interventional
75
1 country
1
Brief Summary
This study investigates whether sharing life stories and creating life-story books can enhance the quality of life and life satisfaction and reduce depression in older adults. The primary research question is: Did the quality of life, life satisfaction, and levels of depression improve more for participants in the intervention group compared to those in the control group? Participants will be divided into two groups:
- Intervention group: These participants will share life stories and create life-story books.
- Control group: These participants will not share life stories or create life-story books.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Oct 2021
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2024
CompletedFirst Submitted
Initial submission to the registry
March 7, 2025
CompletedFirst Posted
Study publicly available on registry
March 18, 2025
CompletedMarch 24, 2025
March 1, 2025
3.2 years
March 7, 2025
March 19, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change from baseline in the depression scores (GDS-15) at 8 weeks
The Geriatric Depression Scale (GDS-15), Arabic version, was used to collect depression scores. It comprises 15 closed-ended questions regarding how the elderly participants felt during the previous week. Zero indicates no depressive symptoms, and 15 indicates severe depressive symptoms.
From enrollment to the end of intervention at 8 weeks.
Secondary Outcomes (2)
Change from baseline in the life satisfaction score at 8 weeks
From enrollment to the end of treatment at 8 weeks
Change from baseline in the quality of life score at 8 weeks
From enrollment to the end of treatment at 8 weeks.
Study Arms (2)
Control
NO INTERVENTIONFive sessions took place at the participants' homes. A self-report questionnaire was used in every session to collect participants' quality of life, life satisfaction, and depression scores.
Life-story review
EXPERIMENTALThe life-story review intervention consisted of five sessions, during which participants shared their life experiences/stories and compiled them into a life-story book. In each session, a self-report questionnaire was administered to assess participants' quality of life, life satisfaction, and levels of depression.
Interventions
There were 5 sessions for the intervention group. All sessions took place in the participant's home. The first 4th sessions involved participant sharing a particular time of their life event, such as childhood, adolescence, adulthood, and the current stage. Transcripts were prepared and compiled following the completion of the interviews. The participants will proofread their life-story book before sending it for printing. In the 5th session, they were given their life storybooks. A self-report questionnaire was used in every session to collect participants' quality of life, life satisfaction, and depression scores.
Eligibility Criteria
You may qualify if:
- aged 60-90;
- depressive symptoms score between 5 and 10;
- able to sign the consent form;
- able to speak Arabic or English;
- able to communicate without the need for a hearing aid.
You may not qualify if:
- using hypnotics, sedatives, antidepressants, anticholinergics, antihistamines, tranquilizers, or melatonin for sleep;
- having a medical diagnosis of Parkinson's, dementia, Alzheimer's disease, or a serious mental problem;
- Participants assigned to the intervention group who did not want to be audio recorded.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Sultan Qaboos University Hospital
Muscat, Muḩāfaz̧at Masqaţ, 123, Oman
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Moon Fai Chan, PhD
Sultan Qaboos University, Department of Family Medicine and Public Health, Muscat, Oman
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
March 7, 2025
First Posted
March 18, 2025
Study Start
October 1, 2021
Primary Completion
November 30, 2024
Study Completion
December 31, 2024
Last Updated
March 24, 2025
Record last verified: 2025-03
Data Sharing
- IPD Sharing
- Will not share
Each participant's life story sharing information is private and confidential, so they did not allow sharing this information with other parties.