CClinicalTrials.gg
CompletedNCT07062653Updated Jul 14, 2025

Comparison of the Effect of Supervised and Non-Supervised Tele-exercise in Women With Diastasis Recti Abdominis

An interventional study of Supervised group and Non-Supervised group in Diastasis Recti Abdominis and Diastasis Recti And Weakness Of The Linea Alba, sponsored by Atlas University. Completed at 1 site in Turkey (Türkiye). Open to female participants aged 18 Years to 45 Years. Per ClinicalTrials.gov, last updated 2025-07-14.

Sponsored by Atlas University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 8 months after the study started (first participant enrolled Jun 2024, registered Feb 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
39
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
Female
01

Study summary

The aim of this study was to determine the effect of supervised and unsupervised telerehabilitation exercise program on inter-rectus distance, abdominal endurance, pelvic floor dysfunction and body image perception in women with diastasis recti abdominis.

Read the detailed description

Rectus abdominis diastasis is defined as the separation of the two rectus abdominis muscles along the linea alba, disrupting the structure of the linea alba. It can be caused by increased volume in the abdominal cavity, hormonal changes during pregnancy, neurodevelopmental differences or abdominal wall laxity. It is very common during pregnancy and can persist in the postpartum period. Loss of abdominal wall stability and weakening of the pelvic floor muscles can occur with DRA. can cause various problems in women. Core stability exercises, pelvic floor training and trunk muscle training are some of the exercise regimen options for the management of DRA. However, to our knowledge, studies on telerehabilitation are insufficient in the literature.

02

Conditions studied

  • Diastasis Recti Abdominis
  • Diastasis Recti And Weakness Of The Linea Alba

Keywords

  • Diastasis recti abdominis
  • tele-coaching
  • tele-exercise
  • postpartum
03

In context

Lead sponsor

Atlas University is the lead sponsor of 91 studies on the registry; 25 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • Post- partum women (min 8 weeks - max 3 years)

Exclusion criteria

Exclusion Criteria:

  • History of abdominal surgery
  • Any neurological disease, systemic musculoskeletal system disease
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
39 participants (actual)

Study arms

  • Experimental
    Supervised group

    The Participants practicing an exercise program where the physiotherapist organizes the exercises through an online platform.

    Other: Supervised group

  • Experimental
    Non-Supervised group

    The Participants practicing the program at home with detailed exercise videos.

    Other: Non-Supervised group

Interventions

  • OtherSupervised group

    A progressive core stability exercise program based on motor control principles will be applied on an online platform through videos under the control of a physiotherapist.

  • OtherNon-Supervised group

    A core stability exercise program with detailed exercise videos will be implemented at home.

06

What researchers measure

Primary outcomes

  1. Inter-recti distance

    The subjects are assessed the inter-recti distance (IRD) in the supine position, knees bent and feet resting position on the table, the subjects is going to be asked to elevate the head and shoulders upwards until the inferior angles of the scapulae were just off the table.The subjects palpated the medial edges of RA muscles and IRD was measured using finger palpation in previously marked five-point: on the umbilicus, 4.5 cm, and 2.5 cm above and below the umbilicus

    Time frame: baseline

  2. Inter-recti distance

    The subjects are assessed the inter-recti distance (IRD) in the supine position, knees bent and feet resting position on the table, the subjects is going to be asked to elevate the head and shoulders upwards until the inferior angles of the scapulae were just off the table.The subjects palpated the medial edges of RA muscles and IRD was measured using finger palpation in previously marked five-point: on the umbilicus, 4.5 cm, and 2.5 cm above and below the umbilicus

    Time frame: after 6 weeks

Secondary outcomes

  1. Abdominal muscle endurance test

    The static abdominal flexion endurance test is also performed once in the same position as the IRD test. The subjects are asked to raise their head and shoulders upwards until the scapulae cleared the table and keep the position as long as possible. The time was recorded as the score of the test.

    Time frame: baseline

  2. Abdominal muscle endurance test

    The static abdominal flexion endurance test is also performed once in the same position as the IRD test. The subjects are asked to raise their head and shoulders upwards until the scapulae cleared the table and keep the position as long as possible. The time was recorded as the score of the test.

    Time frame: after 6 weeks

  3. Pelvic floor dysfunction

    Every subject will complete the Turkish version of the short-form of Pelvic Floor Distress Inventory (PFDI-20) which consists of three subscales: the Pelvic Organ Prolapse Distress Inventory short-form (POPDI6), the Urogenital Distress Inventory short-form (UDI-6), and the Colorectal-Anal Distress Inventory short-form (CRADI-8) to assess prolapse and pelvic pressure, urinary symptoms, and bowel symptoms, respectively

    Time frame: baseline

  4. Pelvic floor dysfunction

    Every subject will complete the Turkish version of the short-form of Pelvic Floor Distress Inventory (PFDI-20) which consists of three subscales: the Pelvic Organ Prolapse Distress Inventory short-form (POPDI6), the Urogenital Distress Inventory short-form (UDI-6), and the Colorectal-Anal Distress Inventory short-form (CRADI-8) to assess prolapse and pelvic pressure, urinary symptoms, and bowel symptoms, respectively

    Time frame: after 6 weeks

  5. Body-self relation

    Every subject will complete the Turkish version of Multi-Dimensional Body-Self Relations Questionnaire.

    Time frame: baseline

  6. Body-self relation

    Every subject will complete the Turkish version of Multi-Dimensional Body-Self Relations Questionnaire.

    Time frame: after 6 weeks

  7. Postnatal Depression

    Every subject will complete the Turkish version of the Edinburgh Postnatal Depression Scale

    Time frame: baseline

  8. Postnatal Depression

    Every subject will complete the Turkish version of the Edinburgh Postnatal Depression Scale

    Time frame: after 6 weeks

  9. balance

    each participant performed a one-leg stand test for the dominant leg

    Time frame: baseline

  10. balance

    each participant performed a one-leg stand test for the dominant leg

    Time frame: after 6 weeks

07

Study locations

1 site
  • Atlas University, İstanbul, Kağıthane 34413
    Istanbul, Turkey (Türkiye)
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 14, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07062653
Lead sponsor
Atlas University
Responsible party
Hilal Denizoğlu Külli (Assoc. Prof., Atlas University) — Principal investigator
First posted
Jul 14, 2025
Start date
Jun 10, 2024
Primary completion
Jul 25, 2024
Completion
Nov 27, 2024
Last update
Jul 14, 2025

Oversight

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

Not currently enrolling

This study is completed, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion