- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01343238
Short- and Longterm Effects of Physical Activity and Dietary Restriction Postpartum (LEVA)
September 8, 2016 updated by: Göteborg University
Short- and Longterm Effects of Physical Activity and Dietary Restriction Postpartum on Women's Weight and Body Composition: a Randomized Study
The study will investigate whether physical exercise, or dietary restrictions, or a combination of both, among overweight and obese postpartum women lead to a significantly larger reduction in weight in a longer perspective, compared to similar women not receiving the intervention.
The study also will investigate the effects on body composition, cardiovascular fitness, blood lipids, insulin levels and inflammation markers.
In total, 68 women with pre-pregnancy BMI 25 - 34.9 will be randomized at 10 wk postpartum into: (1) physical exercise, (2) dietary restrictions, (3) physical exercise + dietary restrictions and (4) control group.
The intervention lasts for 12 wk and longterm effects are measured 1 yr after trial initiation.
To date only studies showing short term (12 wk) effects exist.
Our study is the first to include four intervention groups, so that separate effects of physical activity and dietary restriction and their interaction, can be assessed.
Further, the investigators will estimate effects on body composition taking body water into account and estimate total energy expenditure with higher precision than previously.
Overweight and obesity is an escalating problem in Sweden.
Sustainable weight reduction programs are urgently needed.
During the postpartum period, women may be motivated to lose weight.
Information aimed at promoting life style changes among overweight and obese women could in a longer perspective be integrated in the regular maternal health care in Sweden.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
76
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Gothenburg, Sweden, 40530
- The University of Gothenburg
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- prepregnant BMI 25-35
- non smoking, single term birth
- intention to breastfeed exclusively for 6 mo
Exclusion Criteria:
- Diseases or medication in mother or child
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Diet
12 week diet modification intervention by dietician
|
12 week diet behavior modification
|
Experimental: Exercise
12 week physical exercise modification intervention by physical therapist
|
12 week exercise behavioral intervention
|
Experimental: Diet and Exercise
12 week diet and exercise behavioral modification by dietician and physical therapist
|
12 week diet and exercise behavioral modification intervention
|
No Intervention: Control
Standard procedure
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Body weight
Time Frame: 12 weeks
|
Weight loss after 12 weeks intervention
|
12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
body composition
Time Frame: 12 weeks
|
Change in body composition after 12 weeks intervention
|
12 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Anna Winkvist, PhD, The Unviersity of Gothenburg
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Brekke HK, Bertz F, Rasmussen KM, Bosaeus I, Ellegard L, Winkvist A. Diet and exercise interventions among overweight and obese lactating women: randomized trial of effects on cardiovascular risk factors. PLoS One. 2014 Feb 7;9(2):e88250. doi: 10.1371/journal.pone.0088250. eCollection 2014.
- Hagberg LA, Brekke HK, Bertz F, Winkvist A. Cost-utility analysis of a randomized controlled weight loss trial among lactating overweight/obese women. BMC Public Health. 2014 Jan 15;14:38. doi: 10.1186/1471-2458-14-38.
- Winkvist A, Bertz F, Ellegard L, Bosaeus I, Brekke HK. Metabolic risk profile among overweight and obese lactating women in Sweden. PLoS One. 2013 May 7;8(5):e63629. doi: 10.1371/journal.pone.0063629. Print 2013.
- Bertz F, Brekke HK, Ellegard L, Rasmussen KM, Wennergren M, Winkvist A. Diet and exercise weight-loss trial in lactating overweight and obese women. Am J Clin Nutr. 2012 Oct;96(4):698-705. doi: 10.3945/ajcn.112.040196. Epub 2012 Sep 5.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2007
Primary Completion (Actual)
August 1, 2010
Study Completion (Actual)
June 1, 2011
Study Registration Dates
First Submitted
April 26, 2011
First Submitted That Met QC Criteria
April 27, 2011
First Posted (Estimate)
April 28, 2011
Study Record Updates
Last Update Posted (Estimate)
September 9, 2016
Last Update Submitted That Met QC Criteria
September 8, 2016
Last Verified
September 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- K2009-70X-21091-01-3
- FAS Dnr: 2006-0339 (Other Grant/Funding Number: Swedish Council for Working Life and Social Research)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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