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Abdominal Muscles Recovery Response to Kinesiotaping in Women With Postnatal Diastasis

O

October 6 University

Status

Unknown

Conditions

Diastasis Recti

Treatments

Other: Kinesiotaping
Other: Abdominal Exercises

Study type

Interventional

Funder types

Other

Identifiers

NCT04932772
012/003222

Details and patient eligibility

About

This study aims to investigate abdominal muscle recovery in response to KT by using objective method for assessment as digital caliper, and waist circumference. KT technique will include rectus abdominis, internal and external oblique muscles among females after normal vaginal delivery.

Enrollment

24 estimated patients

Sex

Female

Ages

25 to 35 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age will range from 25-35 years.
  2. All women give birth by normal vaginal delivery.
  3. Diastasis recti more than 2.5 cm at any point along linea alba.
  4. Body mass index (BMI) less than 30 kg/m2.
  5. After the end of Puerperium period i.e. after eight weeks postnatal.

Exclusion criteria

  1. Women with skin over sensitivity to tape.
  2. Women with abdominal skin diseases.
  3. Abdominal hernia.
  4. Previous cesarean section.
  5. Multiple pregnancies more than 3 times.
  6. Other abdominal or back operation.
  7. Pregnancy related complications such as polyhydramnios, fetal macrostomia, diabetes, and hypertension.
  8. Spinal disorders.
  9. Lower limbs deformities.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

24 participants in 2 patient groups

Group A (kinesiotaping group)
Experimental group
Description:
include 24 women will receive kinesiotaping combined with abdominal exercise (2sessions /week for eight weeks).
Treatment:
Other: Abdominal Exercises
Other: Kinesiotaping
Group B (abdominal exercise group)
Active Comparator group
Description:
include 24 women will receive abdominal exercise only.
Treatment:
Other: Abdominal Exercises

Trial contacts and locations

1

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Central trial contact

Mohammed K Sayed Elarabi, Bsc.

Data sourced from clinicaltrials.gov

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