Effect of the 'Mother and Baby' Program on Well-Being

Sponsor
University of Melbourne (Other)
Overall Status
Completed
CT.gov ID
NCT00361478
Collaborator
(none)
160
1
2
13
12.3

Study Details

Study Description

Brief Summary

The study investigates the effect of the 'Mother and Baby' (M&B) program on the psychological health and well-being of new mothers 6-10 weeks following the birth of their baby. The M&B program is an 8-week program of group exercise and education sessions provided by various health professionals. The design of the study is a comprehensive cohort design, including a randomised controlled trial. The primary outcome measure is the Affect Balance Scale. The hypotheses are:

  1. The M&B program has a positive effect on new mothers' psychological health and well-being.

  2. The M&B program increases participation in regular physical activity.

  3. the M&B program benefits first time mothers more than women who have had more than one child.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Exercise and education
  • Behavioral: Education
Phase 3

Detailed Description

Background

The benefits of exercise, in particular group exercise, for women in early motherhood include improved body image, decreased anxiety, improved energy and building of social networks. Exercise has also been shown to be beneficial in the management of mood disorders such as depression and more specifically, postnatal depression. However there has been no suggestion that exercise may reduce symptoms of psychotic disorders that require medication, psychiatric therapy and possible hospitalisation. The number of women experiencing postnatal depression (PND) has increased to one in five women following childbirth. Some of the risks of development of PND include lack of social support during the childbearing year and lack of involvement in the community. new mothers have identified that reasons for inactivity include no child care, limited opportunity to exercise with their baby, reduced self-esteem, poor body image, or they are too busy. Research to date is limited and qualitative in nature, with no standardised measurement tools used to assess quality of life in postnatal women.

The 'Mother and Baby' (M&B) program is an 8-week program involving one hour of group exercise with mothers and their babies conducted by a physiotherapist and a 30-minute education session provided by various health professionals (physiotherapist, nutritionist, speech pathologist, psychologists and midwives). Education topics include baby massage, nutrition for mothers, introducing solids, adjusting to a new lifestyle, communicating with the baby, sun care for the baby and play development. The aim of the study is to explore the benefits of the M&B program on new mothers' psychological and physical well-being as well as the social benefits of exercise.

Research Plan

The design of the study is a comprehensive cohort design incorporating a randomised controlled trial (RCT)of the effects of the M&B program on the health of health women 6-10 weeks following the birth of their baby. The cohort design will complement the results of a classic RCT by allowing the investigation of outcomes in a setting that simulates the 'real-world' treatment process.

Women who have had their babies at the Angliss Hospital and are ready for discharge will be invited to participate in the study. Potential participants will be asked if they have a preference for the M&B program or Education sessions only, or if they would be willing to be part of an RCT. Those who agree to be part of the RCT will be randomised to M&B or Education only sessions. Allocation will be controlled by the chief investigator and will be concealed, with codes placed in opaque sealed enveloped. Randomisation will be stratified according to parity (first time mothers vs multiparous) and blocked in groups of 16.

All participants will receive and complete a questionnaire booklet and will return this in a pre-paid envelope. Questionnaires include:

  1. The Affect Balance Scale. This is the primary outcome measure. It is a highly reliable scale comprising ten questions indicating psychological reactions (positive and negative) to events in daily life.

  2. Edinburgh Postnatal Depression Scale. This is a widely used scale for the detection of risk factors for postnatal depression.

  3. Questions regarding exercise. Three questions regarding exercise will be asked and answers will be compared to tables of the number of metabolic equivalents (METS) required to perform the activity.

  4. Program evaluation. Participants undertaking the M&B program will complete a standardised evaluation form.

Sample size

A preliminary power calculation has been conducted from studies using the Affect Balance Scale in similar settings. With 80 subjects per group we will have 80% power to detect a 1.4 unit difference between the two groups. An advantage of 1.4 units (or 7% to 10% across a scale) is regarded as a clinically important difference. A pilot study will be undertaken to confirm the sample size.

Study Design

Study Type:
Interventional
Actual Enrollment :
160 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Effect of the 'Mother and Baby' Program on New Mothers' Psychological and Physical Well-Being.
Study Start Date :
Jul 1, 2005
Actual Primary Completion Date :
Aug 1, 2006
Actual Study Completion Date :
Aug 1, 2006

Arms and Interventions

Arm Intervention/Treatment
Experimental: 1

"Mother and Baby" Program comprising exercise and education.

Behavioral: Exercise and education
Weekly exercise and education program for 8 weeks
Other Names:
  • Exercise
  • Active Comparator: 2

    Education only

    Behavioral: Education
    Written educational material
    Other Names:
  • Educational material
  • Outcome Measures

    Primary Outcome Measures

    1. Affect Balance Scale [4 weeks]

    Secondary Outcome Measures

    1. Edinburgh Postnatal Depression Scale [4 weeks]

    2. Exercise level [4 weeks]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 45 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Healthy women giving birth at the Angliss Hospital (primiparous and multiparous)
    Exclusion Criteria:
    • Previous history of postnatal depression

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The Angliss Hospital Ferntree Gully Victoria Australia 3156

    Sponsors and Collaborators

    • University of Melbourne

    Investigators

    • Study Director: Mary P Galea, PhD, University of Melbourne
    • Principal Investigator: Emily Ashby, BPhysio, The Angliss Hospital
    • Principal Investigator: Margaret Sherburn, MWHlth, University of Melbourne
    • Principal Investigator: Richard Osborne, PhD, University of Melbourne

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00361478
    Other Study ID Numbers:
    • 07/2004
    First Posted:
    Aug 8, 2006
    Last Update Posted:
    Aug 13, 2008
    Last Verified:
    Jul 1, 2006
    Keywords provided by , ,
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 13, 2008