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Stories in the Moment: Dance Program for People Living With Dementia

NCT06221202 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 72

Last updated 2024-01-24

No results posted yet for this study

Summary

This study is designed to evaluate the impact on the quality of life and wellbeing of a person-centered online dance program on people living with dementia or MCI and care partners.

The duration of the study will be 1 year. Each participant in the study will be followed for approximately 4 months. The study includes joining a weekly 1-hour dance program online on Zoom for 12 weeks. Prior and after the dance program, participants will meet with the research coordinator to answer some questionnaires about wellbeing and reflections on their experience in the program. After the completion of the dance program, participants will be invited to join a focus group to reflect of the impact of the program with fellow participants.

The study will enroll up to 72 participants. This includes 36 dyads of persons living with dementia or MCI and their care partners.

The study will enroll community-dwelling people living with a diagnosis of mild cognitive impairment or mild to moderate-stage dementia and care partners living in the United States.

Conditions

Interventions

OTHER

Stories in the Moment Dance Program - Online

Stories in the Moment is a co-creative dance, movement and storytelling program for persons living with dementia and care partners.

Sponsors & Collaborators

Principal Investigators

  • Magda Kaczmarska, MFA · DanceStream Projects; Global Brain Health Institute

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-02-10
Primary Completion
2024-05-31
Completion
2024-10-31

Countries

  • United States

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06221202 on ClinicalTrials.gov