- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02602106
Regular Aquatic Activities and Pregnancy Outcomes (aquapreg)
Effects of Regular Aquatic Activities on Pregnancy Outcomes
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Rubén O Barakat Carballo, PhD
- Phone Number: 4120 913364120
- Email: barakatruben@gmail.com
Study Contact Backup
- Name: Mariano Bacchi
- Email: marianobacchi@gmail.com
Study Locations
-
-
-
Madrid, Spain, 28040
- Recruiting
- Thecnical University of Madrid
-
Contact:
- Mariano Bacchi
- Email: marianobacchi@gmail.com
-
Contact:
- Rubén Barakat, PhD
- Email: barakatruben@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Healthy pregnant women without any medical or obstetric complication to practice moderate exercise
- Being able to communicate in Spanish
Exclusion Criteria:
- Being interesting in the study after 16 weeks of gestation
- Having obstetric contraindications
- Not attended regular to the exercise program
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Intervention group
The aquatic exercise program included a total of three 50-55 minutes session per week. Pregnant women started at 9 weeks and finished at 38-39 weeks. Each session included 10 minutes of warm up and 10 minutes of cool down including an specific pelvic floor muscle training. The core section of the session included aerobic and strength moderate exercise in water during 25 to 30 minutes |
Women were suggested to exercise regularly through aquatic activities.
A professional in physical exercise and sports designed and conducted the aquatic exercise program.
|
No Intervention: Control group
Sedentary healthy pregnant women
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Maternal gestational weight gain
Time Frame: 40-42 weeks
|
Maternal weight gain was collected at the end of pregnancy as well as before getting pregnant (pre-gestational weight gain)
|
40-42 weeks
|
Birthweight
Time Frame: 37-42 weeks
|
Birth weight was collected at delivery
|
37-42 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of participants with adverse pregnancy outcomes as assessed by medical records
Time Frame: 37-42 weeks
|
Other health baby outcomes at delivery
|
37-42 weeks
|
Gestational age
Time Frame: 37-42 weeks
|
Gestational age of pregnancy
|
37-42 weeks
|
Maternal blood pressure and gestational diabetes as assessed by medical records
Time Frame: 9 to 42 weeks
|
Blood pressure, gestational diabetes...
|
9 to 42 weeks
|
Collaborators and Investigators
Investigators
- Principal Investigator: Ruben Barakat Carballo, PhD, Technical University of Madrid
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- UFLO_UPM_12
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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