MOM-mi: Exploring the Effectiveness of a 12-week Movement Intervention on Heart Rate Variability and Self-compassion Among New Mothers

Sponsor
University of the Fraser Valley (Other)
Overall Status
Recruiting
CT.gov ID
NCT05403983
Collaborator
Les Mills International (Other)
90
1
3
24
3.7

Study Details

Study Description

Brief Summary

This is a mixed-methods randomized controlled trial assessing the effects of an online and in person 12-week movement intervention compared to an education only control group on heart rate variability, self-compassion, psychological well-being, fatigue, exercise self-efficacy, physical activity identity, and body image in postpartum women.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Yoga movement intervention
  • Other: Education booklet
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
90 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
MOM-mi: Exploring the Effectiveness of a 12-week Movement Intervention on Heart Rate Variability and Self-compassion Among New Mothers
Anticipated Study Start Date :
Aug 15, 2022
Anticipated Primary Completion Date :
Aug 15, 2024
Anticipated Study Completion Date :
Aug 15, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: In person movement intervention

In person yoga movement intervention (Les Mills BodyBalance: mixture of yoga, tai chi, pilates) two times per week

Behavioral: Yoga movement intervention
Mixture of yoga, tai chi, pilates. Will be delivered in person (experimental) and online (active comparator)
Other Names:
  • Les Mills BodyBalance
  • Les Mills BodyFlow
  • Active Comparator: Online yoga movement intervention

    Pre-recorded video of yoga movement intervention (Les Mills BodyBalance: mixture of yoga, tai chi, pilates) two times per week

    Behavioral: Yoga movement intervention
    Mixture of yoga, tai chi, pilates. Will be delivered in person (experimental) and online (active comparator)
    Other Names:
  • Les Mills BodyBalance
  • Les Mills BodyFlow
  • Active Comparator: Education

    Education control group using a recently published postpartum physical activity guidebook through the Sport Information Resource Center

    Other: Education booklet
    Recently published postpartum physical activity guidebook through the Sport Information Resource Center of Canada

    Outcome Measures

    Primary Outcome Measures

    1. Heart rate variability [Baseline, 12 weeks]

      Waking RMSDD heart rate variability (chest strap)

    2. Self compassion [Baseline, 12 weeks, 3 months]

      Self-compassion scale

    Secondary Outcome Measures

    1. Physical activity [Baseline, 12 weeks, 3 months]

      Type, amount and frequency of planned exercise, and walking bouts

    2. Self efficacy [Baseline, 12 weeks, 3 months]

      Self-efficacy and barrier to exercise scale

    3. Fear of self-compassion [Baseline, 12 weeks, 3 months]

      Fear of self-compassion scale

    4. Fatigue [Baseline, 12 weeks, 3 months]

      Multidimensional fatigue inventory scale

    5. Sleep quality [Baseline, 12 weeks, 3 months]

      PROMIS sleep questionnaire

    6. Perceived stress [Baseline, 12 weeks, 3 months]

      Perceived stress scale

    7. Physical activity identify [Baseline, 12 weeks, 3 months]

      Athlete identity measurement scale

    8. Body image [Baseline, 12 weeks, 3 months]

      Body dissatisfaction scale

    9. Motivation for exercise [Baseline, 12 weeks, 3 months]

      Psychological needs for exercise scale

    10. Postpartum depression [Baseline, 12 weeks, 3 months]

      Edinburgh postnatal depression scale

    11. Anxiety [Baseline, 12 weeks, 3 months]

      State-trait anxiety scale

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    19 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Women who have given birth to a child within the past 6 months and who are cleared for physical activity by their health care provider.
    Exclusion Criteria:
    • Participants who have a medical condition that precludes them passing the Get Active questionnaire

    • Women not clear for physical activity by a health care provider

    • Participants who are not able to attend classes at pre-specified times

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of the Fraser Valley Chilliwack British Columbia Canada V2R0N3

    Sponsors and Collaborators

    • University of the Fraser Valley
    • Les Mills International

    Investigators

    • Principal Investigator: Iris Lesser, PhD, University of the Fraser Valley
    • Principal Investigator: Gillian Hatfield, PhD, University of the Fraser Valley
    • Principal Investigator: Amanda Wurz, PhD, University of the Fraser Valley

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Gillian Hatfield, Associate Professor, University of the Fraser Valley
    ClinicalTrials.gov Identifier:
    NCT05403983
    Other Study ID Numbers:
    • 101075
    First Posted:
    Jun 3, 2022
    Last Update Posted:
    Jun 3, 2022
    Last Verified:
    May 1, 2022
    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

    Study Results

    No Results Posted as of Jun 3, 2022