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Clinical Trials/NCT02906956
NCT02906956CompletedPhase 1

Music and Adherence in Upper Extremity Home Programs Post Stroke

Duquesne University1 site in 1 country7 target enrollmentStarted: September 1, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 1
Status
Completed
Enrollment
7
Locations
1
Primary Endpoint
Duration of sessions of practice

Study Overview

Brief Summary

The purpose of this study is to explore whether adherence to upper extremity home programs changes when persons post stroke practice with preferred music.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
40 Years to 85 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Ages 40-85
  • •Mild to Moderate hemiparesis as determined by a score of 21 to 50 on the FM- UE
  • •At least 6 months post stroke
  • •American English as primary language

Exclusion Criteria

  • •Significant visual impairment as determined by "aphasia-friendly" and age appropriate screening
  • •Significant hearing impairment as determined by self-report
  • •Actively receiving occupational or physical therapy services for upper extremity motor recovery
  • •Severe auditory comprehension impairment such that they cannot understand one-step directions as indicated by a WAB-R score below 8/10 on Sequential Commands Subtest
  • •Sitting or standing blood pressure of 180/110 or HE > 100 bpm

Arms & Interventions

Preferred Music Playlist

Experimental

All participants will have this phase twice in the protocol. See description in intervention section.

Intervention: Preferred music playlist (Behavioral)

Outcomes

Primary Outcomes

Duration of sessions of practice

Time Frame: 4 weeks

Number of minutes of practice

Time Frame: 4 weeks

Number of sessions of practice

Time Frame: 4 weeks

Secondary Outcomes

  • Cognitive Linguistic Quick Test(Baseline)
  • Canadian Occupational Performance Measure(Baseline and no more than one week post intervention period)
  • Motor Activity Log(Baseline and no more than one week post intervention period)
  • Western Aphasia Battery - Revised(Baseline)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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