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The Music Activity INTervention for Adherence Improvement Through Neurological Entrainment (MAINTAIN)

Primary Purpose

Myocardial Infarction, Compliance Behavior, Patient Compliance

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Preference Based Rhythmic Auditory Stimulation Music
Preference Based Music Intervention
Sponsored by
Toronto Rehabilitation Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Myocardial Infarction

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • English-speaking patients, who are participating in and have been declared medically stable for out-patient cardiac rehabilitation, will be recruited from the Toronto Rehabilitation Institute's Cardiac Rehabilitation and Secondary Prevention Program.

Exclusion Criteria:

  • Participants who are unable to wear the MP3 device or the activity monitoring device due to medical or non-medical issues will be excluded from this study.
  • Subjects that have a medical history of seizure disorders, previous neurosurgery, or known head trauma will be excluded from this study.
  • Subjects that have received a bicycle-based exercise prescription.

Sites / Locations

  • Toronto Cardiac Rehabilitation Institute

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Active Comparator

Active Comparator

Arm Label

Standard

Preference Based Music Intervention

Preference Based Rhythmic Auditory Stimulation Music

Arm Description

Subjects randomized to this group will receive standard, usual care with no intervention.

Subjects randomized to this arm will receive an iPod player and an activity monitoring device. The iPod will be loaded with patient indicated music preferences that is synched to the patients pace prescription. Subjects will be asked to use their iPod player during off-site exercise periods.

Subjects randomized to this arm will receive an iPod player and an activity monitoring device. The iPod will be loaded with patient indicated music preferences that is synched to the patients pace prescription. Subjects will be asked to use their iPod player during off-site exercise periods. Rhythmic Auditory Stimulation (accentuation of beats, frequencies) will be added to the music subliminally.

Outcomes

Primary Outcome Measures

Duration of physical activity
The primary outcome will be the total weekly physical activity volume as determined using triaxial accelerometers.

Secondary Outcome Measures

On-site program attendance
Adherence will be measured quantitatively by assessing the number of missed appointments vs. amount of scheduled appointments.
Change in Cardio Pulmonary Assessment Score
Fitness levels will be measured by assessing peak VO2 (ml/kg-1* min-1), an objective, clinical measure of the volume of oxygen consumed while exercising at the maximum capacity. Those with higher VO2max values are more fit and can exercise more intensely, indicating a greater functional capacity than those with lower VO2max values.
Changes in Stafford Self-Efficacy Questionnaire/Cardiac Self-Efficacy Questionnaire Scores
Changes in self efficacy will be measured using the combined score of two self-efficacy questionnaires administered by Toronto Rehabilitation Institute
Audio-play list use
We will track the number of song plays on each patients playlist
Study recruitment and drop-out
We will determine the proportion of patients screened, recruited, and who completed the study protocol

Full Information

First Posted
December 3, 2012
Last Updated
October 8, 2020
Sponsor
Toronto Rehabilitation Institute
Collaborators
Ontario Centres of Excellence, University of Toronto
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1. Study Identification

Unique Protocol Identification Number
NCT01752595
Brief Title
The Music Activity INTervention for Adherence Improvement Through Neurological Entrainment
Acronym
MAINTAIN
Official Title
The Music Activity INTervention for Adherence Improvement Through Neurological Entrainment Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
November 2012 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
December 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Toronto Rehabilitation Institute
Collaborators
Ontario Centres of Excellence, University of Toronto

4. Oversight

5. Study Description

Brief Summary
Auditory motor-coupling has been shown to induce neural-entrainment that can synchronize walking-pace with sonic tempo. The extent to which acoustical-motor entrainment can induce longer-term changes to physical activity behaviours remains unclear. Cardiac rehabilitation is essential and is associated with irrefutable mortality benefits for patients following an acute cardiac event. Randomized clinical trials have demonstrated a 25-50% improvement in survival as compared to controls; however, as many as 50% of patients will dropout of such programs prior to completion, which undermines these morbidity and mortality benefits (37; 54). Research exploring ways to improve compliance to such programs has suggested that the incorporation of music and other such holistic, patient-centered interventions into a rehabilitation/exercise program is associated with improved motivation, endurance and satisfaction amongst cardiac rehabilitation participants. The MAINTAIN study has been designed to conduct a feasibility evaluation on the effects of a preference-based music intervention on adherence to the cardiac rehabilitation program at Toronto Rehabilitation Institute. The primary objective of the trial is to evaluate the feasibility of the implementation of such a protocol within the context of the program. This is a two-arm, block 2:1 randomized trial. 35 patients participating in cardiac rehabilitation at Toronto Rehabilitation: Cardiac Rehabilitation and Secondary Prevention Program will be recruited and participants will be randomized into: 1) control (standard, usual care); and, 2) music intervention. The randomization process employed will be a blocked 2:1 strategy, whereby subjects are randomized to the music treatment arms 2:1. All those patients randomized into arm 2 will be equally randomized into either (2) preference-based music intervention, (3) preference-based music enhanced with RAS. The primary outcome measure will be weekly physical activity over a 3 month duration as measured using tri-axial accelerometers. We will also analyze the impact of a preference-based music intervention based on audio playlist utilization, self-reported sitting times ,exercise-times, on-site attendance to the cardiac rehabilitation program (attendance), peak oxygen uptake (VO2) (stress-test), and self-efficacy levels (self-efficacy questionnaires). These measures will be collected and analyzed throughout the course of the intervention (3 months).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myocardial Infarction, Compliance Behavior, Patient Compliance

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
34 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard
Arm Type
No Intervention
Arm Description
Subjects randomized to this group will receive standard, usual care with no intervention.
Arm Title
Preference Based Music Intervention
Arm Type
Active Comparator
Arm Description
Subjects randomized to this arm will receive an iPod player and an activity monitoring device. The iPod will be loaded with patient indicated music preferences that is synched to the patients pace prescription. Subjects will be asked to use their iPod player during off-site exercise periods.
Arm Title
Preference Based Rhythmic Auditory Stimulation Music
Arm Type
Active Comparator
Arm Description
Subjects randomized to this arm will receive an iPod player and an activity monitoring device. The iPod will be loaded with patient indicated music preferences that is synched to the patients pace prescription. Subjects will be asked to use their iPod player during off-site exercise periods. Rhythmic Auditory Stimulation (accentuation of beats, frequencies) will be added to the music subliminally.
Intervention Type
Behavioral
Intervention Name(s)
Preference Based Rhythmic Auditory Stimulation Music
Intervention Description
Patients that have been randomized into arms 2 and 3 will be blinded to the intervention they are receiving (i.e. preference-based playlist vs. preference-based playlist that has been edited to include Rhythmic Auditory Stimulation (RAS). RAS drives synchronous neural oscillation (entrainment) and functions in two ways: (1) facilitates pace and heart-rate synchrony and (2) facilitates brain state dominance (getting into the zone). RAS will be accomplished through: (1) sequencing of subject self-selected music based on tempo, (2) accentuation of the rhythmic driving pulse with added percussive-type sounds, (3) addition of binaurally detuned pitches to follow bass lines at brain-state target frequencies (e.g., 8 Hz alpha, or 16 Hz beta), and (4) the addition of binaurally detuned "background" sounds (e.g., low frequency hum) at target Hz frequencies. RAS is implemented as inherent and natural to the music and may remain imperceptible to most.
Intervention Type
Other
Intervention Name(s)
Preference Based Music Intervention
Primary Outcome Measure Information:
Title
Duration of physical activity
Description
The primary outcome will be the total weekly physical activity volume as determined using triaxial accelerometers.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
On-site program attendance
Description
Adherence will be measured quantitatively by assessing the number of missed appointments vs. amount of scheduled appointments.
Time Frame
3 months
Title
Change in Cardio Pulmonary Assessment Score
Description
Fitness levels will be measured by assessing peak VO2 (ml/kg-1* min-1), an objective, clinical measure of the volume of oxygen consumed while exercising at the maximum capacity. Those with higher VO2max values are more fit and can exercise more intensely, indicating a greater functional capacity than those with lower VO2max values.
Time Frame
Baseline, 3 months
Title
Changes in Stafford Self-Efficacy Questionnaire/Cardiac Self-Efficacy Questionnaire Scores
Description
Changes in self efficacy will be measured using the combined score of two self-efficacy questionnaires administered by Toronto Rehabilitation Institute
Time Frame
Baseline, 3 months
Title
Audio-play list use
Description
We will track the number of song plays on each patients playlist
Time Frame
3 months
Title
Study recruitment and drop-out
Description
We will determine the proportion of patients screened, recruited, and who completed the study protocol
Time Frame
3 months
Other Pre-specified Outcome Measures:
Title
Interview and Focus Group
Description
Tertiary outcomes of the study will include information gathered regarding music playlist preferences and subjective opinions about the role of music in exercise programs through post-intervention interviews (attached). Other secondary outcomes include the energy expenditure and activity time as recorded over the entire three-month period by the activity monitoring device and MP3 device (this data collected every 2 weeks).
Time Frame
3 months

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: English-speaking patients, who are participating in and have been declared medically stable for out-patient cardiac rehabilitation, will be recruited from the Toronto Rehabilitation Institute's Cardiac Rehabilitation and Secondary Prevention Program. Exclusion Criteria: Participants who are unable to wear the MP3 device or the activity monitoring device due to medical or non-medical issues will be excluded from this study. Subjects that have a medical history of seizure disorders, previous neurosurgery, or known head trauma will be excluded from this study. Subjects that have received a bicycle-based exercise prescription.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr. David Alter
Organizational Affiliation
Toronto Rehabilitation Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Toronto Cardiac Rehabilitation Institute
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M4G 1R7
Country
Canada

12. IPD Sharing Statement

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The Music Activity INTervention for Adherence Improvement Through Neurological Entrainment

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