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After Cesarean Time Interval for Exercise (ACTIVE) Trial

After Cesarean Time Interval for Exercise (ACTIVE) Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04345757
Acronym
ACTIVE
Enrollment
200
Registered
2020-04-14
Start date
2020-11-01
Completion date
2025-09-01
Last updated
2026-02-27

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

Conditions

Postoperative Complications

Keywords

Postpartum wellness, Postoperative activity, Postoperative complication, Postpartum complication

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.

Interventions

The exercise program will be designed by a physical therapist (Ms. Patricia Ladis) who specializes in postnatal rehabilitation and will be supervised by sports medicine physicians from the Hospital For Special Surgery (HSS). The structured program will include approximately 10 minutes of core muscle group exercises. They will begin this program 2 weeks after their cesarean section. The study group will perform these exercises 5 times per week.

Sponsors

Weill Medical College of Cornell University
Lead SponsorOTHER
Hospital for Special Surgery, New York
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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.

Exclusion criteria

* 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)

Design outcomes

Primary

MeasureTime frameDescription
Change in wellness2, 6, and 10 weeksAs 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

MeasureTime frameDescription
Change in incidence of post operative complications2, 6, and 10 weeksAs 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
Change in incidence of depression, anxiety, and decreased physical functioning2, 6, and 10 weeksAs 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.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORRobin Kalish, MD

Weill Medical College of Cornell University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026