NCT00486629Active, not recruiting
Impact of Diet and Exercise Activity on Pregnancy Outcomes
Impact of a Community-based Obesity and Diabetes Prevention Program on Pregnant Outcomes in Pregnant Women
Source: ClinicalTrials.gov · Last updated 8 Jan 2026
Brief summary (registry, in English)
The general goal of the present study is to assess the impact of a community-based exercise and dietary intervention in pregnant women living in urban areas during and after their pregnancy on the reduction of the risks of both diabetes and obesity in mothers and their offspring. We hypothesize that a community-based lifestyle intervention program during and after gestation may improve pregnancy outcomes in terms of reducing the risk of developing obesity or type 2 DM in mothers and their children.
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 1000 (estimated)
- First submitted
- 12 Jun 2007
- Start date
- Jul 2004
- Primary completion date
- Jun 2027
- Lead sponsor
- University of Manitoba
- Diseases
- Obesity, Type 2 diabetes
- NCT number
- NCT00486629
What you commit to
- Study type: Interventional
- Planned participants: 1000
- From Jul 2004 to the primary completion date, Jun 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Obstetric or medical contraindications for exercise according to 2002 SOCG guideline (ruptured membranes, preterm labor, incompetent cervix, hypertensive disorders of pregnancy, growth restricted fetus, placenta previa, persistent bleeding in 2nd or 3rd trimester, significant metabolic, cardiovascular, respiratory or systemic disorder) (5, 6).
- Pre-existing diabetes (except a history of GDM, but not in current pregnancy).
Other
- Multiple gestations.
Who the study is looking for
- Pregnancy \< 20 weeks.
- Expressed interest in study and willingness to consent to participate in the study.
Age in the registry: 18 years to - · Sex: Female · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of Manitoba Coordinator of this site? Confirm its status | Winnipeg | Canada | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.