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A Lifestyle Program on Healthy Weight in Postpartum Period

Development and Evaluation of a Lifestyle Intervention Program for Women' Weight Reduction After Childbirth

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02620059
Enrollment
100
Registered
2015-12-02
Start date
2016-09-01
Completion date
2017-10-30
Last updated
2018-05-01

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

Conditions

Weight Reduction

Keywords

Postpartum Period

Brief summary

The aim of this study is to examine the impact of lifestyle intervention on postpartum weight loss. So the investigators will have two groups in this study. In Experimental group women will receive the Healthy Lifestyle Intervention. This intervention will have been delivered during 12 weeks. In Control group women will receive general information via pamphlet about postpartum period and tips for stress management.

Detailed description

This study will be conducted in two phases. In the first phase , the investigators will conduct a cross-sectional study to assess factors related to the healthy lifestyle after childbirth based on the PRECEDE model. Regarding results of the study, the investigators will plan and implement a lifestyle promoting intervention and will evaluate the effect of the intervention on weight reduction among postpartum women.

Interventions

BEHAVIORALLifestyle Intervention

The investigators will provide information on healthy eating and physical activity. They will give pedometers to the participants to monitor their daily steps in order to increase it till 10000 steps/day.

Sponsors

Tehran University of Medical Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Singleton pregnancy * Lactating * Non-smoking * Full-term birth * Lack of medical problems * Lack of any pregnancy-related complications (eg, multiple pregnancy, fetal anomalies, fetal or maternal complications in current or previous pregnancy, and hypertension in pregnancy). * Nonparticipation in other studies which may affect the results. * 18.5≤ BMI≤29 before pregnancy * Women who are sedentary according to the International Physical Activity Questionnaire.

Exclusion criteria

* Unwilling to continue participation in the study * Pregnancy during the study * Suffering physical problems during the study * Smoking after birth

Design outcomes

Primary

MeasureTime frameDescription
Body weight changesChanges from baseline at 12 months postpartumThe investigators will assess body weight changes through BMI (kg/m2)

Secondary

MeasureTime frameDescription
Dietary intake changesChanges from baseline at 12 months postpartumThe investigators will assess dietary intake changes with 24 hours dietary recall.
Physical activity changesChanges from baseline at 12 months postpartumThe pedometer will measure the number of steps.

Other

MeasureTime frameDescription
Postpartum weight retention changesChanges from baseline at 12 months postpartumPostpartum weight retention will be measured by calculating the difference between weight at a certain time in the postpartum period and weight before pregnancy using a weight scale.
Stress management changesChanges from baseline at 12 months postpartumStress will be assessed by the Health Promoting Lifestyle Profile (Adult Version) Scale.
Cognitive changes based on the selected behavior change model/sChanges from baseline at 12 months postpartumCognitive changes will be assessed through questionnaire developed based on behavior change model/s.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026