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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05619718
Other study ID # 12528
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 23, 2024
Est. completion date September 30, 2025

Study information

Verified date March 2024
Source Lawson Health Research Institute
Contact Serena Wong, PhD
Phone 519-455-5110
Email serena.wong@sjhc.london.on.ca
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this pilot study is to determine the feasibility and acceptability of a group loneliness intervention in geriatric psychiatry inpatients. This type of group loneliness intervention is based on functional analytic psychotherapy and is called Awareness, Courage, and Love Groups.


Description:

The objective of our clinical trial is to adapt, implement, and evaluate a type of loneliness group intervention called Awareness, Courage, and Love Groups for older adults in a psychiatric unit. The following research questions will be answered: (a) Are ACL groups with geriatric psychiatry inpatients feasible and acceptable? (b) Do such ACL groups demonstrate preliminary efficacy?


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date September 30, 2025
Est. primary completion date August 25, 2025
Accepts healthy volunteers No
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria: - Admission to geriatric psychiatry inpatient unit Exclusion Criteria: - Individuals who are disoriented to person, delirious, unable to tolerate or participate meaningfully in the group, or otherwise unable to provide consent to research and psychotherapy

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Awareness, Courage, and Love Groups
Groups based on the Awareness, Courage, and Love framework from functional analytic psychotherapy
Other:
Mutual Help Meetings
Groups based on treatment as usual where patients gather to discuss how they can help others on the ward, and make requests for how others can help them.

Locations

Country Name City State
Canada Parkwood Institute Mental Health London Ontario

Sponsors (2)

Lead Sponsor Collaborator
Lawson Health Research Institute Western University, Canada

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Other Satisfaction Questionnaire Brief open-ended questions about program satisfaction. Responses are qualitative. Up to 2 months
Primary Inclusion of Other in the Self Scale (IOS) Brief single-item pictorial measure of social closeness. The minimum value is 1, the maximum value is 7, and higher scores indicate a better outcome. Up to 2 months
Primary UCLA Loneliness Scale (ULS-6) Brief measure of loneliness. The minimum value is 6, the maximum value is 24, and higher scores indicate a worse outcome. Up to 2 months
Primary Relational Health Indices (RHI) Brief measure of group relational health. The minimum value is 8, the maximum value is 40, and higher scores indicate a better outcome. Up to 2 months
Primary Quantitative Program Satisfaction Brief measure of program satisfaction. The minimum value is 0, the maximum value is 16, and higher scores indicate a better outcome. Up to 2 months
Secondary Cantril Self-Anchoring Striving Scale 1 item pictorial scale of subjective wellbeing from 0 (minimum) to 10 (maximum). A higher score indicates a better outcome. Up to 2 months
Secondary Sacred Moment Qualities (SMQ) Brief measure of perceived sacred qualities, adapted from Pargament et al. (2014). The minimum value is 11, the maximum value is 55, and higher scores indicate a better outcome. Up to 2 months
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