MASTER: Music After Stroke To Enhance Rehabilitation

Sponsor
Pace University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04441515
Collaborator
Emory University (Other)
12
3
32

Study Details

Study Description

Brief Summary

Music that is familiar and preferred by patients has been shown to heighten neuroplasticity and can mitigate these disabilities. Therefore, this study seeks to explore the effect of providing patient preferred music to patients in the very early post stroke period (within 24 hours of a left cerebral artery stroke [LMCA]event) as a complementary modality to usual stroke care.

Condition or Disease Intervention/Treatment Phase
  • Device: Ipod with music
  • Device: ipod with books to listen
  • Device: ipod only with usual care
N/A

Detailed Description

Aim I. The primary aim of MASTER is to identify whether a potential relationship exists between an intervention of participant preferred music, when initiated within the first 24 hours following a left middle cerebral artery stroke, and a reduction in the following disabilities: Expressive aphasia, right hand functional deficit and post stroke depression. This aim will serve to address the first research hypothesis and address the relationship between These disabilities are well known sequalae among patients diagnosed with the most common form of stroke, a LMCA stroke. Participant preferred music within the first 24 hours following a LMCA stroke and a reduction in: Expressive aphasia, right hand functional deficit and post stroke depression, as these disabilities are well known sequalae among LMCA stroke patients.

Aim II. The second aim of MASTER is to identify if a relationship exists between an intervention of audible books, when initiated within the first 24 hours following a LMCA stroke, and a reduction in the following disabilities: Expressive aphasia, right hand functional deficit and post stroke depression.

Sufficient evidence exists to suggest that although listening to books stimulates cognitive function, the effect of melody and participant engagement in music is far superior to listening to words alone as the inherent rhythmicity of patient-favored music has been shown to strengthen synchronous neuronal connectivity, by modulating dopamine and inducing fine grained neuroanatomical changes in a recovering brain.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
12 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Music After Stroke To Enhance Rehabilitation
Anticipated Study Start Date :
Apr 30, 2021
Anticipated Primary Completion Date :
Oct 30, 2023
Anticipated Study Completion Date :
Dec 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Music

music supplied by ipod

Device: Ipod with music
music of patient's preference provided 2 hours daily

Active Comparator: oral books

Listening to books on ipod

Device: ipod with books to listen
2 hours of daily listening to books

Placebo Comparator: usual care

Usual care

Device: ipod only with usual care
participants given device only

Outcome Measures

Primary Outcome Measures

  1. expressive aphasia measured by use of the WAB-R [6 months]

    Change in expressive aphasia will be measured by use of the WAB-R. Western Aphasia Battery-Revised (WAB- R).This instrument is intended to provide a standardized measure of aphasia type and severity. Implementation of the instrument takes 15 approximately minutes to complete. THE WAB-R identifies and classifies 8 aphasia types: Global, Broca's, Isolation, Transcortical Motor, Wernicke's, transcortical Sensory, Conduction and Anomic. The WAB-R assesses linguistic skills more frequently affected by aphasia. Participants will be assessed at enrollment, discharge from hospital and again at 1,3,6 months post stroke.

  2. motor activity right hand as measured using the Motor Activity log [6 months]

    Change in right hand motor activity and function will be assessed using the Motor Activity Log. The Motor Activity Log (MAL) is a semi-structured interview for hemiparetic stroke patients to assess the use of their paretic arm and hand Target tasks include object manipulation (e.g. pen, fork, comb, and cup) as well as the use of the arm during gross motor activities (e.g. transferring to a car, steadying oneself during standing, pulling a chair into a table while sitting). Participants will be assessed at enrollment, discharge from hospital and again at 1,3,6 months post stroke.

  3. Depressive symptoms as measured using the PHQ-9 [6 months]

    A change in depressive symptoms will be assessed using the PHQ-9. The PHQ-9 will be used for screening for depression, as it has been identified as the preferred (gold standard) screening tool for depression among post stroke patients in hospitals. The PHQ-9 takes less than 5 minutes to administer, and has been shown to have superior sensitivity and specificity.

  4. Quality of life as measured using the 20 item short form survey (SF-20) [6 months]

    Change quality of life is assessed in this study, a 20-item short form survey (SF-20) will be used to assess quality of life. Participants will be assessed at enrollment, discharge from hospital and again at 1,3,6 months post stroke.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Clinical diagnosis of LMCA stroke within prior 24 hours

  • Not identified as critically ill

  • Glascow Coma Scale > 8 at time of consent

  • Resident of a home with a land line or cell phone

  • Able to speak in English or Spanish prior to stroke event

  • Presence of expressive aphasia at time of enrollment.

Exclusion Criteria:
  • Stroke diagnosis other than LMCA territory stroke

  • Unable to provide consent by patient or legally accountable person acting on behalf of the patient (healthcare proxy, healthcare power of attorney), Patient/ representative

  • Does not speak English or Spanish prior to stroke event

  • Have a diagnosis of end stage cancer, or other medical conditions that dramatically increase a risk of mortality within one year

  • Any pre-existing communication disorder (including dementia)

  • Patients that are deemed critically ill will not be included

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Pace University
  • Emory University

Investigators

  • Principal Investigator: Millie Hepburn, PhD, Pace University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Pace University
ClinicalTrials.gov Identifier:
NCT04441515
Other Study ID Numbers:
  • MASTER1
First Posted:
Jun 22, 2020
Last Update Posted:
Mar 11, 2021
Last Verified:
Mar 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 11, 2021