- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05977608
The Impact of a Telephone Reminiscence Program
The Impact of a Telephone Reminiscence Program on Reminiscence Functions and Mental Health Outcomes in Community-Dwelling Older Adults
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The prevalence of social isolation and loneliness among older adults is a public health problem. It is reported that 25 % of community-dwelling older adults 65 and older are socially isolated while 43 % of older adults 60 and older feel lonely (Cudge et al., 2020). Research has shown that social isolation and loneliness are associated with cardiovascular disease, stroke, depression, dementia, and mortality (Holjlerda, 2016). Loneliness, in particular, has been identified as a potential predictor of mild cognitive impairment (Bundy, et al., 2021; Sutin et al., 2018; Dahlberg, 2021). As a result of the prevalence data, gerontologists and researchers have cited the need for developing, implementing and testing innovative interventions to address this problem. Reminiscence is one example of a cost-effective intervention shown to decrease loneliness and improve mental health and wellness.
STORII is a telephone reminiscence program designed to provide a service that automatically calls older adults three times a week asking them meaningful questions about their lives. The participants have the opportunity to select curated prompts that enable them to record their life stories through the phone. The participants can choose to share them online with their families. Through formative evaluation of the program, the STORII team has noted that their participants to be highly satisfied and highly engaged. As a result of these informal data, it was decided that a more in-depth investigation should be undertaken. Therefore, the purpose of this study is to examine the impact of the STORII program on reminiscence functions and mental health outcomes in community-dwelling older adults.
Participants will be invited to join a telephone reminiscence program designed to provide a service that automatically calls older adults three times a week asking them meaningful questions about their lives. Examples of the questions are "What is the best meal you have ever tasted?", "What is one of your proudest moments?", "What is your earliest memory?". Participants can share as much or as little as they would like. They have up to 10 minutes to record the answers and can end the call at any time by hanging up. There will be no operator on the line that can hear or respond. The participants can choose to share their stories online with their families.
All outcome measures will be assessed at baseline (T0), 6-week post-test (T1), and at 12-week follow-up (T2). Participants will complete assessments via phone, by trained research assistants using four questionnaires. Assessments will be completed by research assistants who are not aware of participants' allocation.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Juliette Shellman, PhD
- Phone Number: 860-212-4044
- Email: juliette.shellman@uconn.edu
Study Locations
-
-
Connecticut
-
Storrs, Connecticut, United States, 06269
- Recruiting
- University of Connecticut
-
Contact:
- Juliette Shellman, PhD
- Phone Number: 860-212-4044
- Email: juliette.shellman@uconn.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 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
Exclusion Criteria:
- Significant hearing loss
- Cognitive impairment
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Group 1
Participants will be asked to participate in the reminiscence program during the first 6 weeks of the study.
|
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.
|
Experimental: Group 2
Participants will be asked to participate in the reminiscence program during the second 6 weeks of the study.
|
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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in Mental health as measured by mean changes in the Mental Health Continuum Short Form (MHC-SF) scores
Time Frame: Baseline, Week 6 (Endpoint), Week 12 (Follow up)
|
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)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in reminiscence functions as measured by mean changes in the Modified Reminiscence Functions Scale (MRFS) scores
Time Frame: Baseline, Week 6 (Endpoint), Week 12 (Follow up)
|
The Modified Reminiscence Functions Scale (MRFS) containing 29 items will be used to measure reminiscence functions.
The scale measures the frequency of different reminiscence functions identified as: (a) self-regard, (b) death preparation, (c) bitterness revival, (d) conversation, and (e) intimacy maintenance, teach and inform, boredom reduction, and conversation.
Respondents are asked to report their level of agreement with statements such as, "When I reminisce, it is to teach younger people about cultural values" or "When I reminisce, recalling my past help me know who I am now" on a 5-point scale ranging from 1 (never) to 5 (very often).
A higher score indicates more frequent reminiscences for the specific function.
The Cronbach's Alpha for the subscales ranged from .73 to .91,
indicating good internal consistency (Shellman & Zhang, 2014; Washington, 2009).
|
Baseline, Week 6 (Endpoint), Week 12 (Follow up)
|
Change from loneliness as measured by mean changes in UCLA 3 Item Loneliness Scale scores
Time Frame: Baseline, Week 6 (Endpoint), Week 12 (Follow up)
|
UCLA 3 Item Loneliness Scale (UCLA 3) (Russell, 1996) is a brief 3-item scale that measures three dimensions of loneliness: relational connectedness, social connectedness, and self.
Responses are provided on a 3-point response scale ranging from "hardly" to "often", with total scores ranging from 3 to 9. Higher scores indicate a higher level of loneliness.
The instrument has favorable psychometric properties, including high internal consistency (ranging from 0.89 to 0.94) and a good test-retest reliability over one year (r = .73)
(Russell, 1996).
|
Baseline, Week 6 (Endpoint), Week 12 (Follow up)
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Change from life satisfaction as measured by mean changes in the Satisfaction with Life Scale scores
Time Frame: Baseline, Week 6 (Endpoint), Week 12 (Follow up)
|
The Satisfaction with Life Scale (SWLS) (Diener et al., 1985) is a measure of life satisfaction that includes five statements, such as "In most ways, my life is close to my ideal."
Responses are provided on a seven-point scale ranging from (1) "strongly disagree" to (7) "strongly agree", with a total score ranging from 7 to 35.
Higher scores indicate greater life satisfaction.
The scale is a highly reliable measure, with good internal consistency (0.87) and high test-retest reliability over a 2-month period (r = .82)
(Diener et al., 1985).
|
Baseline, Week 6 (Endpoint), Week 12 (Follow up)
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Collaborators and Investigators
Sponsor
Collaborators
Publications and helpful links
General Publications
- 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.
- 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.
- Keyes CL. The mental health continuum: from languishing to flourishing in life. J Health Soc Behav. 2002 Jun;43(2):207-22.
- 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.
- 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.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- H23-0046
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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