[Remote] Beyond Listening: A music-based intervention

  • STATUS
    Recruiting
  • End date
    Mar 31, 2022
Updated on 16 June 2021
Investigator
Kendra Ray, PhD
Primary Contact
[Remote] Beyond Listening: A music-based intervention (5.0 mi away) Contact
+241 other location

Summary

1.This study is for people with dementia and their family caregiver. 
2. The intervention is a 6-week psychoeducational, music-based workshop designed for caregivers of PWD. The caregiver will attend a one-hour, online session for 6 consecutive weeks. Caregivers will implement a daily caregiving routine that incorporates singing, music with movement and listening to relaxing music that will aid in reducing undesirable behaviors and create pleasurable interactions between caregivers and their spouses living at home with Alzheimer's or related dementias. 
3. Anyone in the NYC area may participate. 
4. Informed consent will be required. Additionally, questionnaires before and after the study will be requested to be completed by the caregiver. 
5. The study is free of charge. All dyads will receive a portable speaker and an iPod for use and participation during the study.

Description

There will be one baseline visit, and two post tests (immediately following study and 3 months after). Each of these visits will take about 30 minutes. There will be 6 psychoeducational sessions that will last for one hour and will be held each week.

Study activities for caregivers may include: Answering questions over the phone Attending an online workshop with a music therapist once a week for one hour Singing, moving to music, or playing music for the care recipient twice a week for 30 minute Study activities for care recipients may include: Listening to music Engaging in music-based activities with caregiver

Details
Condition Dementia
Clinical Study IdentifierTX271575
Last Modified on16 June 2021

Eligibility

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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