After Cesarean Time Interval for Exercise (ACTIVE) Trial
- Conditions
- Postoperative Complications
- Interventions
- Behavioral: Structured exercise
- Registration Number
- NCT04345757
- Lead Sponsor
- Weill Medical College of Cornell University
- Brief Summary
The purpose of this study is to test whether or not activity restrictions after a cesarean section are warranted and if exercise can improve postpartum wellness. This research study is being done because there is no science-based evidence to support postpartum activity restrictions after cesarean sections.
Participants will be randomly placed into one of the following study groups:
* Standard postpartum and post-operative instructions group: activity restrictions, including no strenuous exercise, sexual intercourse, or lifting objects greater than 25 pounds for 6 weeks or until evaluation at the 6 week postpartum visit
* Study group: Structured 10 week exercise protocol consisting of core strengthening exercises (concentrating on the abdominal, gluteal, and pelvic areas), breathing exercises, and diaphragm exercises.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- Female
- Target Recruitment
- 200
- pregnant woman at least 18 years of age
- carrying only one baby at time of delivery
- delivery planned by scheduled cesarean section
- baby of gestational age of > 37 weeks
- no known restrictions to exercise.
- woman with pre-existing post operative complications
- medical history with exercise limitations/disabilities
- carrying more than one baby at time of delivery
- delivery (planned by scheduled or emergent) cesarean section with fetal concerns (anomaly, growth restriction, NICU admission, etc)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Study Group Structured exercise Study group: Structured 10 week exercise protocol
- Primary Outcome Measures
Name Time Method Change in wellness 2, 6, and 10 weeks As measured by scores in the completion of the PROMIS GSF assessment.
The PROMIS GSF assessment uses a method of scoring requiring responses to each item for each participant. Each question usually has five response options ranging in value from one to five. All questions must be answered in order to produce a valid score using the scoring tables. A score of 50 is the average for the United States general population with a standard deviation of 10. A higher PROMIS T-score represents more of the concept being measured. For negatively-worded concepts like Anxiety, a T-score of 60 is one SD worse than average. By comparison, an Anxiety T-score of 40 is one SD better than average. However, for positively-worded concepts like Physical Function-Mobility, a T-score of 60 is one SD better than average while a T-score of 40 is one SD worse than average.
- Secondary Outcome Measures
Name Time Method Change in incidence of depression, anxiety, and decreased physical functioning 2, 6, and 10 weeks As measured by scores in the completion of the PROMIS GSF assessment.
The PROMIS GSF assessment uses a method of scoring requiring responses to each item for each participant. Each question usually has five response options ranging in value from one to five. All questions must be answered in order to produce a valid score using the scoring tables. A score of 50 is the average for the United States general population with a standard deviation of 10. A higher PROMIS T-score represents more of the concept being measured. For negatively-worded concepts like Anxiety, a T-score of 60 is one SD worse than average. By comparison, an Anxiety T-score of 40 is one SD better than average. However, for positively-worded concepts like Physical Function-Mobility, a T-score of 60 is one SD better than average while a T-score of 40 is one SD worse than average.Change in incidence of post operative complications 2, 6, and 10 weeks As measured by number of subjects presenting with any of the following:
* Wound separation, dehiscence, hernia etc.
* Re-hospitalization for wound concerns
* Infection
* Increased pain, abdominal/core muscle injury
* Less breastmilk production (adequate-inadequate, Likert scale 1-5)
* Urinary incontinence
* Improved fitness
Trial Locations
- Locations (1)
New York Presbyterian Hospital Weill Cornell
🇺🇸New York, New York, United States