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A community lifestyle programme to improve the well-being of pregnant women with a body mass index (BMI) of 30 kg/m^2 or more

A community lifestyle programme to improve the well-being of pregnant women with a body mass index (BMI) of 30 kg/m^2 or more: a feasibility study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN29860479
Enrollment
400
Registered
2010-04-22
Start date
2009-09-01
Completion date
Unknown
Last updated
2016-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Weight gain during pregnancy Pregnancy and Childbirth Other maternal diseases classifiable elsewhere but complicating pregnancy, childbirth and the puerperium

Interventions

Women will be recruited to the study as soon after their booking appointment as possible (after 12 weeks gestation). They will be invited to attend a 10-week community lifestyle programme before 30 we

Sponsors

University of Manchester (UK)
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Female aged 18 years or over 2. Pregnant 3. Booking BMI of 30 kg/m^2 or more 4. Patient at Royal Bolton or Royal Oldham Hospital

Exclusion criteria

Exclusion criteria: 1. Booking BMI of less than 30 kg/m^2 2. Aged under 18 years 3. Intend to move in the next three months 4. Take weight control medication 5. Have been advised by a Health care professional to not take part in physical activity during their pregnancy 6. Have any cautions for starting exercise (using the Revised Physical Activity Readiness Questionnaire [PARQ]) and the Royal College of Obstetricians and Gynaecologists [RCOG])

Design outcomes

Primary

MeasureTime frame
1. Weight gain during pregnancy, weighed at booking and at the end of the pregnancy 2. Pregnancy outcome data (e.g., birth weight and mode of delivery), measured at end of the pregnancy

Secondary

MeasureTime frame
1. Psychological outcomes including self-efficacy, well-being and goal attainment: measured at four timepoints in questionnaire (baseline, start of the 10-week programme, end of the 10-week programme and 4 - 6 week postpartum follow-up) 2. Women's experience of pregnancy and health care services: measured at four timepoints in questionnaire (baseline, start of the 10-week programme, end of the 10-week programme and 4 - 6 week postpartum follow-up) and daily diary from recruitment to 1 - 6 weeks postpartum 3. Amount of physical activity: measured at four timepoints in questionnaire (baseline, start of the 10-week programme, end of the 10-week programme and 4 - 6 week postpartum follow-up) and daily diary from recruitment to 1 - 6 weeks postpartum 4. Food intake: measured at four timepoints in questionnaire (baseline, start of the 10-week programme, end of the 10-week programme and 4 - 6 week postpartum follow-up) and daily diary from recruitment to 1 - 6 weeks postpartum 5. The suitability and acceptability of the intervention components: measured post-programme in the end of programme questionnaire and post-partum follow-up questionnaire and focus group

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 19, 2026