Music and Adherence Home Programs Post Stroke

Stroke Clinical Trial

Official title:

Music and Adherence in Upper Extremity Home Programs Post Stroke

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02906956
• Other study ID #: #2016/06/18
• Status: Completed
• Phase: Early Phase 1
• Start date: September 2016
• Est. completion date: August 2017

Study information

• Verified date: July 2019
• Source: Duquesne University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 7
• Est. completion date: August 2017
• Est. primary completion date: August 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years to 85 Years

Eligibility

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

Related Conditions & MeSH terms

• Stroke

Intervention

Behavioral:
• Preferred music playlist
Client will be instructed in a home program based on repetitive task practice principles and will complete this program with and without the use of a preferred music playlist during practice.

Locations

Country	Name	City	State
United States	Duquesne University Speech, Hearing, Language Clinic	Pittsburgh	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
Duquesne University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Qualitative Feedback Interview	One-to-one interview with supported communication strategies on the experience of the intervention and study materials.	No more than 3 weeks post intervention period
Other	Intensity of Practice	Rate of accelerations as measured by an activity monitor	4 weeks
Primary	Number of sessions of practice		4 weeks
Primary	Duration of sessions of practice		4 weeks
Primary	Number of minutes of practice		4 weeks
Secondary	Canadian Occupational Performance Measure	Perceived occupational performance on activities of importance to the client	Baseline and no more than one week post intervention period
Secondary	Motor Activity Log	Perceived amount and quality of use of the affected upper extremity	Baseline and no more than one week post intervention period
Secondary	Western Aphasia Battery - Revised	Measure of language impairment	Baseline
Secondary	Cognitive Linguistic Quick Test	Measure of cognition	Baseline