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Examining the Effects of (MiM) Treatment on Emotional and Cognitive Functioning of Residents in Long-term Care

Examining the Effects of (MiM) Treatment on Emotional and Cognitive Functioning of Residents in Long-term Care

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02219620
Acronym
MiM
Enrollment
30
Registered
2014-08-19
Start date
2014-08-31
Completion date
2016-05-31
Last updated
2016-06-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Emotion, Impaired Cognition

Keywords

creative arts, older adults, intervention study

Brief 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.

Detailed 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.

Interventions

BEHAVIORALMusic, Imagery, Movement

Implementation of music, art and imagery activation, and movement in group modality

BEHAVIORALSocial Control

social conversational group facilitated by care counselor

Sponsors

George Mason University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
emotional functioningpre-post 10 week treatment and 6 week FU

Secondary

MeasureTime frame
cognitive functioningpre-post 10 week intervention and 6 week FU

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026