After Cesarean Time Interval for Exercise (ACTIVE) Trial

Sponsor
Weill Medical College of Cornell University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04345757
Collaborator
Hospital for Special Surgery, New York (Other)
600
1
2
26
23.1

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Structured exercise
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
600 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
After Cesarean Time Interval for Exercise (ACTIVE) Trial
Actual Study Start Date :
Nov 1, 2020
Anticipated Primary Completion Date :
Oct 1, 2022
Anticipated Study Completion Date :
Jan 1, 2023

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Standard instructions

Standard instructions: 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

Experimental: Study Group

Study group: Structured 10 week exercise protocol

Behavioral: Structured exercise
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.

Outcome Measures

Primary Outcome Measures

  1. Change in wellness [2, 4, 6, 8, and 12 weeks]

    As measured by scores in the completion of the PROMIS29 assessment. The PROMIS29 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

  1. Change in incidence of post operative complications [2,4,6,8,and 12 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

  2. Change in incidence of depression, anxiety, and decreased physical functioning [2,4,6,8,and 12 weeks]

    As measured by scores in the completion of the PROMIS29 assessment. The PROMIS29 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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts 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 due to fetal concerns (anomaly, growth restriction, NICU admission, etc)

Contacts and Locations

Locations

Site City State Country Postal Code
1 New York Presbyterian Hospital Weill Cornell New York New York United States 10021

Sponsors and Collaborators

  • Weill Medical College of Cornell University
  • Hospital for Special Surgery, New York

Investigators

  • Principal Investigator: Robin Kalish, MD, Weill Medical College of Cornell University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Weill Medical College of Cornell University
ClinicalTrials.gov Identifier:
NCT04345757
Other Study ID Numbers:
  • 19-11021020
First Posted:
Apr 14, 2020
Last Update Posted:
Mar 31, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Weill Medical College of Cornell University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 31, 2022