NCT05977608

Brief Summary

The purpose of this study is to better understand how a telephone reminiscence program impacts reminiscence functions and mental health outcomes in community-dwelling older adults.This study will take 12 weeks to complete and will include approximately 90 study participants. Participants will be randomly assigned to one of two telephone reminiscence groups.They will be either assigned to begin a telephone reminiscence program immediately or in 6 weeks. Participants will receive automatic calls three times a week asking the meaningful questions about their lives. At week 1, week 6, and week 12, participants will also be asked to complete assessments via phone, by research assistants using four questionnaires.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
90

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jun 2023

Shorter than P25 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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 25, 2023

Completed
17 days until next milestone

First Submitted

Initial submission to the registry

July 12, 2023

Completed
23 days until next milestone

First Posted

Study publicly available on registry

August 4, 2023

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2023

Completed
Last Updated

July 18, 2025

Status Verified

July 1, 2025

Enrollment Period

6 months

First QC Date

July 12, 2023

Last Update Submit

July 15, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Change in Mental health as measured by mean changes in the Mental Health Continuum Short Form (MHC-SF) scores

    The Mental Health Continuum Short Form (MHC-SF) (Keyes, 2002) will be used to assess mental health and well-being. The 14 item scale measures emotional, social, and psychological dimensions of mental health. Participants answer each item on a 6-point scale, ranging from 0 and 5, resulting in a total score between 0 to 70. The emotional well-being subscale has a range from 0 to 15, the social well-being subscale scores range from 0 to 25, and the psychological well-being subscale scores range from 0 to 30. Higher scores on MHC- SF indicate a higher level of mental well-being. The MHC-SF has demonstrated excellent internal consistency (\>.80) and discriminant validity in adults in the United States (Keyes, 2005, 2006), and its test-retest reliability has also been demonstrated, with an average of 0.68 over three consecutive three-month periods and 0.65 over a 9-month period (Lamers et al., 2011).

    Baseline, Week 6 (Endpoint), Week 12 (Follow up)

Secondary Outcomes (3)

  • Change in reminiscence functions as measured by mean changes in the Modified Reminiscence Functions Scale (MRFS) scores

    Baseline, Week 6 (Endpoint), Week 12 (Follow up)

  • Change from loneliness as measured by mean changes in UCLA 3 Item Loneliness Scale scores

    Baseline, Week 6 (Endpoint), Week 12 (Follow up)

  • Change from life satisfaction as measured by mean changes in the Satisfaction with Life Scale scores

    Baseline, Week 6 (Endpoint), Week 12 (Follow up)

Study Arms (2)

Group 1

EXPERIMENTAL

Participants will be asked to participate in the reminiscence program during the first 6 weeks of the study.

Behavioral: Telephone Reminiscence Intervention

Group 2

EXPERIMENTAL

Participants will be asked to participate in the reminiscence program during the second 6 weeks of the study.

Behavioral: Telephone Reminiscence Intervention

Interventions

Participants will receive automatic calls three times a week asking their life experiences and personal memories. They can share as much or as little as they would like. They have up to 10 minutes to record their answer and can end the call at any time by hanging up.They will be able to share the stories online with their families if they want.

Group 1Group 2

Eligibility Criteria

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

You may qualify if:

  • Adults age \>60 years;
  • English speaking
  • Community-dwelling
  • Willing to participate in a 12 week study
  • Willing and able to share memories using a telephone, 10 minutes, 3 times a week

You may not qualify if:

  • Significant hearing loss
  • Cognitive impairment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Connecticut

Storrs, Connecticut, 06269, United States

Location

Related Publications (5)

  • Keyes CL. The mental health continuum: from languishing to flourishing in life. J Health Soc Behav. 2002 Jun;43(2):207-22.

    PMID: 12096700BACKGROUND
  • Diener E, Emmons RA, Larsen RJ, Griffin S. The Satisfaction With Life Scale. J Pers Assess. 1985 Feb;49(1):71-5. doi: 10.1207/s15327752jpa4901_13.

    PMID: 16367493BACKGROUND
  • Russell DW. UCLA Loneliness Scale (Version 3): reliability, validity, and factor structure. J Pers Assess. 1996 Feb;66(1):20-40. doi: 10.1207/s15327752jpa6601_2.

    PMID: 8576833BACKGROUND
  • Shellman JM, Zhang D. Psychometric testing of the Modified Reminiscence Functions Scale. J Nurs Meas. 2014;22(3):500-10. doi: 10.1891/1061-3749.22.3.500.

    PMID: 25608435BACKGROUND
  • Cudjoe TKM, Roth DL, Szanton SL, Wolff JL, Boyd CM, Thorpe RJ. The Epidemiology of Social Isolation: National Health and Aging Trends Study. J Gerontol B Psychol Sci Soc Sci. 2020 Jan 1;75(1):107-113. doi: 10.1093/geronb/gby037.

    PMID: 29590462BACKGROUND

MeSH Terms

Conditions

Psychological Well-BeingSocial Isolation

Condition Hierarchy (Ancestors)

Personal SatisfactionBehaviorSocial Behavior

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

July 12, 2023

First Posted

August 4, 2023

Study Start

June 25, 2023

Primary Completion

December 31, 2023

Study Completion

December 31, 2023

Last Updated

July 18, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share

Locations