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Active, not recruitingNCT07150897abdominal rebUpdated Sep 2, 2025

Early Rehabilitation of Abdominal Muscle Wall Following Lower Transverse Abdominal Incision

An interventional study of exercise for lower abdominal muscle wall in All Participants Are Post Operative Women After Their 1st Cesarean Delivery or Hysterectomy, sponsored by Beni-Suef University. Active, not recruiting at 1 site in Egypt. Open to female participants aged 35 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-09-02.

Sponsored by Beni-Suef University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Oct 2025, 11 months ago, but the record still lists the study as active, not recruiting.
  • Registered 4 months after the study started (first participant enrolled Apr 2025, registered Aug 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
35 Years to 50 Years
Sex
Female
01

Study summary

to investigate effect of inducing rehabilitation program very early after lower abdominal transverse incisions on abdominal muscles.

Read the detailed description

Abdominal surgery is a general term used to denote surgical procedures conducted in the abdominal area to detect and treat a presenting medical problem.1 Open Abdominal surgery includes vertical and transverse incisions. Low transverse abdominal incision is usually made 1-2 fingerbreadths above the pubic crest with an incision length of 10-14 cm. The lower transverse abdominal incision is adequate for the vast majority of caesarean operations as well as operative disease of the uterus, fallopian tubes, and ovaries. Historically, the gynaecologist- obstetrician has favoured lower abdominal transverse incisions. Several disadvantages of these incisions exist such as limited exploration of the upper abdomen, greater blood loss as well as they are more susceptible to hematoma formation when compared with a midline incision. Paresthesia of the overlying skin results from nerve injury, is more common in a transverse incision compared with a midline incision.2 With regards to the abdominal muscle, there is a relevant surgical related muscle loss induced by major surgical trauma after lower transverse incisions.3 Early postoperative days are associated with fatigue and limited respiratory movements. For the patient, less post operative pain, rapid return to normal function as well as better scar appearance and quality of life are very important factors. Encouraging early mobilization after low transverse abdominal surgery is crucial for optimal healing and recovery of abdominal muscles. In physical therapy, activities such as, transferring from bed to chair, sitting upright, rising from a chair, exercises in or out of bed and walking in the room are considered helpful for surgical patient.4 Up till now, there is no study searched the effect of starting rehabilitation programs for abdominal muscles very early within the first 24 hours after obstetrics and gynaecology surgeries.

02

Conditions studied

  • All Participants Are Post Operative Women After Their 1st Cesarean Delivery or Hysterectomy

Keywords

  • Abdominal Incision, Early Rehabilitation
03

In context

Lead sponsor

Beni-Suef University is the lead sponsor of 333 studies on the registry; 116 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
35 Years to 50 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion Criteria:a total of 60 women will be recruited from the obstetrics and gynecology Department of Beni-Suef University Hospital, Beni-Suef, Egypt. Their ages will be ranged from 35-50 years and their body mass index (BMI) will not exceed 29 kg/m2. All participants are post operative women after their 1st cesarean delivery or hysterectomy.

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Exclusion Criteria:Women will be excluded from the study, if they were diagnosed with heart diseases, respiratory diseases causing excessive coughing or sneezing, chronic physical or mental illness, had more than 1 cesarean delivery; had any medical condition that would prohibit active abdominal muscle contraction; or failed to complete an informed consent form.

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05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Care provider)
Enrollment
60 participants (actual)

Study arms

  • No intervention
    placebo group

    routine postnatal care as well as wear the same belly band and receive advice

  • Experimental
    intervention

    Group A (study group) included participants who join a rehabilitation program starting from day 1 after surgery up to 6 weeks with wearing a belly band

    Other: exercise for lower abdominal muscle wall

Interventions

  • Otherexercise for lower abdominal muscle wall

    the exercise session will start with light walking for 5 minutes followed by, posture correction exercises from crock lying, supine, and sitting and standing positions (each exercise will be maintained for 5 seconds and then the woman relaxed for 10 seconds and repeated each exercise 10 times) to overcome the effect of poor pregnancy posture. Then, participants will perform first step of prone plank exercises which is a stable prone plank with attention to maintain a neutral position in the hip joints, pelvis and lumbar spine. The feet will be placed to match the width of the hip and forearm and acted as support points. The elbows place under the glenohumeral joints, and the arms support the body vertically to the surface. Second step of prone plank exercises will involve performing the unilateral stable prone plank which is the same as the stable prone plank but with the dominant leg in a fully extended position. Third step includes, prone bridge on a Swiss Ball with a diameter of 65

    Also known as: Exercise group

06

What researchers measure

Primary outcomes

  1. ultrasonography

    All assessments will be performed by using a two-dimensional ultrasound diagnostic scanner with a linear probe (Toshiba Xario100, 8-12 MHz linear transducer) to measure thickness of lower part of Rectus Abdominis muscle below umbilicus before and after 6 weeks of the intervention procedure for all participants.

    Time frame: 4 months

07

Study locations

1 site
  • Beni suef university
    Cairo, 02, Egypt
08

References and documents

Individual participant data

Plan to share: No — for safty

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 2, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07150897
Lead sponsor
Beni-Suef University
Responsible party
mohamed naeem (assistant professor, Beni-Suef University) — Principal investigator
First posted
Sep 2, 2025
Start date
Apr 17, 2025
Primary completion
Oct 17, 2025 (estimated)
Completion
Nov 17, 2025 (estimated)
Last update
Sep 2, 2025

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Aug 2025. You cannot join it, but the record below documents what was studied.

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