NCT06881914

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
75

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Oct 2021

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
3.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 30, 2024

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2024

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

March 7, 2025

Completed
11 days until next milestone

First Posted

Study publicly available on registry

March 18, 2025

Completed
Last Updated

March 24, 2025

Status Verified

March 1, 2025

Enrollment Period

3.2 years

First QC Date

March 7, 2025

Last Update Submit

March 19, 2025

Conditions

Keywords

DepressionLife satifactionQuality of lifeOlder adults

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 INTERVENTION

Five 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

EXPERIMENTAL

The 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.

Behavioral: Intervention group:

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.

Life-story review

Eligibility Criteria

Age60 Years - 90 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Depression

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehavior

Study Officials

  • Moon Fai Chan, PhD

    Sultan Qaboos University, Department of Family Medicine and Public Health, Muscat, Oman

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: Intervention group: There were 5 sessions for the intervention group. All sessions took place in the participant's home. In the first 4 sessions, the participant was asked to share their childhood, adolescence, adulthood, and current stage. Transcripts were prepared and compiled following the completion of the interviews. Before printing, participants were asked to add their selected pictures to the life-story book. In the 5th session, they received their life story-story books. A self-report questionnaire was used in every session to collect participants' quality of life, life satisfaction, and depression scores. Control group: The control group had 5 sessions, and participants' quality of life, life satisfaction, and depression scores were collected at each interview only.
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.

Locations