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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02219620
Other study ID # 14-953118
Secondary ID
Status Completed
Phase N/A
First received July 28, 2014
Last updated June 20, 2016
Start date August 2014
Est. completion date May 2016

Study information

Verified date June 2016
Source George Mason University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

To examine the effects of a music, imagery, and movement (MiM) intervention on emotional and cognitive functioning in residents living in a community-based adult long-term care facility.

Hypothesis 1: Residents who participate in the MiM group will improve in emotional functioning, as compared to residents in the control group.

Hypothesis 2: Residents who participate in the MiM group will improve in cognitive functioning, as compared to residents in the control group.


Description:

To implement a community-based integrated music, art and imagery, and movement intervention to improve mood and promote cognitive functioning in older adult residents living in a long-term care facility.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date May 2016
Est. primary completion date May 2016
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Resident in assisted living at long-term care facility with MMSE score above 20

Exclusion Criteria:

- co-morbid psychiatric diagnosis and/or staff clinical evaluation that determines inappropriateness for study inclusion

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Music, Imagery, Movement
Implementation of music, art and imagery activation, and movement in group modality
Social Control
social conversational group facilitated by care counselor

Locations

Country Name City State
United States Assisted Living at Birmingham Green Manassas Virginia

Sponsors (1)

Lead Sponsor Collaborator
George Mason University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary emotional functioning pre-post 10 week treatment and 6 week FU No
Secondary cognitive functioning pre-post 10 week intervention and 6 week FU No
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