20 Participants NeededMy employer runs this trial

Rehabilitation for Cesarean Section Recovery

AB
Overseen ByAndreas Bergdahl, PhD
Age: Any Age
Sex: Female
Trial Phase: Academic
Sponsor: Concordia University, Montreal
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

Cesarean section is the most common inpatient surgical procedure worldwide, with rates continuing to rise; in Canada, approximately one in three births occur by cesarean. Despite its prevalence, there are no expectations for individuals who have undergone a cesarean section to seek out rehabilitation care. Physical recovery guidance and return to activity from a cesarean birth is poorly understood and inadequately supported, with most research focusing on immediate post-operative pain management within the hospital settings. Little attention has been given to long term physical recovery.

Scar-related problems - such as tight or stuck scar tissue, sensitivity or discomfort around the scar, weakness in the abdominal muscles, and infertility or digestive complications - can severely affects the ability to complete daily activities and affect overall quality of life. Rehabilitation is a common and important part of recovery after most major orthopedic and abdominal surgeries. It can help reduce pain and complications, improve mobility, strength, and confidence in movement, and support a gradual return to physical activity. Just as importantly, rehabilitation helps individuals safely resume everyday responsibilities such as caring for their family, returning to work, and managing daily tasks.

The purpose of this study is to examine whether one form of hands-on therapy results in greater improvements in scar comfort, mobility, and performance of daily activities compared with an alternative approach, when both are delivered alongside an identical exercise program.

Participants will take part in an 8-week rehabilitation program following cesarean birth. Rehabilitation will be provided one-on-one by a qualified healthcare professional and will include a combination of in-person sessions and virtual (online) check-ins. In-person sessions will include education about recovery, hands-on therapy, and guided exercises. Virtual sessions will be used to answer questions, review progress, and ensure that exercises are being performed safely and correctly at home.

To evaluate changes in recovery over time, participants will attend three assessment sessions: at baseline (week 0), mid-intervention (week 4), and post-intervention (week 8). During these sessions, researchers will collect information on:

* How the scar looks and moves

* The sensitivity or discomfort of the scar area

* How easily participants can perform everyday movements, such as standing up from a chair

* How participants feel about their scar, pain levels, and daily function There will be two forms off assessments. One that measures the objective changes: photographs of the scar, gentle pressure testing to measure sensitivity, simple movement tests, and ultrasound imaging, while the other form of assessment is patient reported questionnaires about how they feel they are improving. Ultrasound is a safe and painless technique that allows researchers to see how tissues under the skin are healing and moving.

The anticipated benefit of this research is to improve understanding of physical recovery after cesarean birth. The results may help inform future rehabilitation recommendations and contribute to better support for individuals recovering from cesarean surgery.

Are You a Good Fit for This Trial?

This trial is for people who have recently had a cesarean section (C-section) and are experiencing issues like scar discomfort, hip pain, or trouble with movement. Participants should be able to attend both in-person and virtual rehab sessions over an 8-week period.

Inclusion Criteria

Have had 1 or more cesarean births
Have had a cesarean birth within the past 6 months
I have new pain or discomfort at my C-section scar since surgery.
See 4 more

Exclusion Criteria

I have had cancer before.
I do not have uncontrolled diabetes or other untreated hormone disorders.
Currently pregnant, actively undergoing fertility treatment, or planning pregnancy during the study intervention period
See 5 more

What Are the Treatments Tested in This Trial?

Interventions

  • Direct scar massage
  • Indirect massage group

Trial Overview

The study compares two types of hands-on scar massage therapy—direct versus indirect—each combined with the same exercise program. Sessions include education, guided exercises, and regular check-ins over eight weeks to see which approach helps recovery most.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: Direct scar massage groupExperimental Treatment1 Intervention
Group II: Indirect massageActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Concordia University, Montreal

Lead Sponsor

Trials
30
Recruited
5,200+