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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05996718
Other study ID # P30AG064200
Secondary ID DBSR-11114
Status Completed
Phase N/A
First received
Last updated
Start date October 25, 2023
Est. completion date May 20, 2024

Study information

Verified date June 2024
Source Georgia State University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goals of this clinical trial are to: 1) refine the training program, "Improving Care though Improv;" and 2) test the program for its influence self-perceived caregiving mastery (i.e., how persons assess their ability to provide care) among informal caregivers of persons living with moderate dementia. Forty-three informal caregivers will be involved in testing the training program. These individuals will be assigned to groups of between 8 to12 caregivers and take part in weekly 2-hour sessions held over a 4-week period. These caregivers will be taught improvisational (improv) theater skills, which involves being in the moment, self-awareness, and responsiveness to others. This group also will be asked to answer surveys questions about themselves and the person receiving care at three timepoints and invited to provide feedback on their training experiences.


Recruitment information / eligibility

Status Completed
Enrollment 43
Est. completion date May 20, 2024
Est. primary completion date May 20, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Actively engaged in the care of community-dwelling persons living with moderate dementia (4 or 5 on a 7-point dementia-staging scale) who is not likely to be institutionalized within the next 6 months - Able to attend at least 3 of the 4 in-person sessions - Ability to communicate in English

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Training program pilot
This intervention for informal caregivers consists of training that will introduce participants to improvisational (improv) theatre and teach its core communication skills.

Locations

Country Name City State
United States Georgia State University Atlanta Georgia

Sponsors (2)

Lead Sponsor Collaborator
Georgia State University National Institute on Aging (NIA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pearlin Mastery, Loss, and Competence: Caregiver Competence Subscale 4-item Likert-type scale; scores range from 4 to 16 with higher scores indicating greater feelings of competence. at baseline, upon training completion (Week 4), and three months post baseline.
Secondary Perceived Stress Scale 14-item Likert-type scale. Scores range from 0 to 56 with higher scores indicating greater stress. at baseline, upon training completion (Week 4), and three months post baseline.
Secondary Center for Epidemiological Studies-Depression Scale 20-item Likert-type scale. Scores range from 0 to 60 with higher scores indicating greater depression. at baseline, upon training completion (Week 4), and three months post baseline.
Secondary State-Trait Anxiety Inventory 20-item Likert-type scale. Scores range from 20 to 80 with higher scores indicating greater anxiety. at baseline, upon training completion (Week 4), and three months post baseline.
Secondary Zarit Burden Inventory 22-item scale with 4-point Likert scale responses. Scores range from 0 to 88 with higher scores indicating greater burden. at baseline, upon training completion (Week 4), and three months post baseline.
Secondary Revised Memory and Behavioral Problems Checklist 24-item scale with 4-point Likert scale responses. Scores range from 0 to 96 with higher scores indicating greater behavioral expressions observed by caregivers among persons living with dementia. at baseline, upon training completion (Week 4), and three months post baseline.
Secondary Quality of Life-Alzheimer's Disease Scale 13 items with a 4-point Likert scale. Scores range from 13 to with 52 with higher scores indicating greater quality of life among persons living with dementia at baseline, upon training completion (Week 4), and three months post baseline.
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