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MAINTAIN: The Music Activity INTervention for Adherence Improvement Through Neurological Entrainment

Sponsor
Toronto Rehabilitation Institute (Other)
Overall Status
Completed
CT.gov ID
NCT01752595
Collaborator
Ontario Centres of Excellence (Industry), University of Toronto (Other)
34
Enrollment
1
Location
3
Arms
13
Duration (Months)
2.6
Patients Per Site Per Month

Study Details

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).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Preference Based Rhythmic Auditory Stimulation Music
  • Other: Preference Based Music Intervention
 N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
34 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
The Music Activity INTervention for Adherence Improvement Through Neurological Entrainment Study
Study Start Date :
Nov 1, 2012
Actual Primary Completion Date :
Dec 1, 2013
Actual Study Completion Date :
Dec 1, 2013

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Standard

Subjects randomized to this group will receive standard, usual care with no intervention.
Active Comparator: Preference Based Music 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.

Other: Preference Based Music Intervention
Active Comparator: Preference Based Rhythmic Auditory Stimulation Music

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.

Behavioral: Preference Based Rhythmic Auditory Stimulation Music
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.

Outcome Measures

Primary Outcome Measures

  1. Duration of physical activity [3 months]

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

Secondary Outcome Measures

  1. On-site program attendance [3 months]

    Adherence will be measured quantitatively by assessing the number of missed appointments vs. amount of scheduled appointments.

  2. Change in Cardio Pulmonary Assessment Score [Baseline, 3 months]

    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.

  3. Changes in Stafford Self-Efficacy Questionnaire/Cardiac Self-Efficacy Questionnaire Scores [Baseline, 3 months]

    Changes in self efficacy will be measured using the combined score of two self-efficacy questionnaires administered by Toronto Rehabilitation Institute

  4. Audio-play list use [3 months]

    We will track the number of song plays on each patients playlist

  5. Study recruitment and drop-out [3 months]

    We will determine the proportion of patients screened, recruited, and who completed the study protocol

Other Outcome Measures

  1. Interview and Focus Group [3 months]

    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).

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Toronto Cardiac Rehabilitation Institute Toronto Ontario Canada M4G 1R7

Sponsors and Collaborators

  • Toronto Rehabilitation Institute
  • Ontario Centres of Excellence
  • University of Toronto

Investigators

  • Principal Investigator: Dr. David Alter, Toronto Rehabilitation Institute

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Dr. David Alter, Dr. David Alter, MD, PhD, FRCPC, Toronto Rehabilitation Institute
ClinicalTrials.gov Identifier:
NCT01752595
Other Study ID Numbers:
  • 12-035
First Posted:
Dec 19, 2012
Last Update Posted:
Oct 9, 2020
Last Verified:
Oct 1, 2020
Additional relevant MeSH terms:
Myocardial Infarction
Infarction

Study Results

No Results Posted as of Oct 9, 2020