Diastasis Recti AbdominisDRA-SCNCT07458412
Impact of Diastasis Recti Abdominis on Spinal Curvature in Postpartum Women
An observational study of Diastasis Recti Abdominis and Lumbar Lordosis, run by Cairo University.
Trial summary
This study investigates the relationship between diastasis recti abdominis and spinal curvature in postpartum women using non-invasive assessment methods. Read more about this study
- Who is it for?
- Ages 21 to 35 years, women only
- Conditions the study is for
- Diastasis Recti Abdominis, Lumbar Lordosis, Thoracic Kyphosis
- How many people
- 110 participants
- Where
- No sites listed yet
- Study dates
- 2 Mar 2026to 27 Apr 2026
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 21 to 35 years
- Women only
- Adult
Study population: The study population will include postpartum women who meet the eligibility criteria. Participants will be divided into two groups based on the presence or absence of diastasis recti abdominis and will undergo non-invasive assessment of spinal curvature for comparative analysis.
Who may be able to join
- Age range: 21 to 35 years
- BMI between 18 and 29.9 kg/m².
- Normal vaginal delivery or cesarean section.
- Postpartum period between 6 weeks and 6 months
- Participants with or without diastasis recti abdominis (DRA) as determined by ultrasound.
Who cannot join
- • History of spinal deformities (e.g., scoliosis, kyphosis, spondylolisthesis).
- Any neuromuscular or neurological disorders.
- Previous abdominal or spinal surgery.
- Multiple pregnancies.
- Participants currently undergoing physical therapy treatment for spinal or abdominal conditions.
- Inability to comply with instructions or complete the assessment protocol
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
This study investigates the relationship between diastasis recti abdominis and spinal curvature in postpartum women using non-invasive assessment methods.
Read the detailed description
Postpartum musculoskeletal changes are common and may significantly affect spinal alignment and overall physical function. Diastasis recti abdominis (DRA), a separation of the abdominal muscles after pregnancy, is frequently reported among postpartum women and may contribute to alterations in trunk stability and posture. Despite its high prevalence, the potential association between DRA and spinal curvature has not been sufficiently clarified. Understanding this relationship is important, as changes in spinal alignment-such as increased lumbar lordosis or thoracic kyphosis-may influence pain, functional ability, and long-term musculoskeletal health. Therefore, further investigation is needed to better define the connection between DRA and spinal curvature in order to support early assessment and improve postpartum rehabilitation strategies.
- Medical subject headings
- Lordosis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Women with Diastasis Recti | Postpartum women diagnosed with diastasis recti abdominis. Participants will undergo non-invasive assessment of spinal curvature for comparison purposes. No intervention will be administered. | |
| Women without Diastasis Recti | Postpartum women without diastasis recti abdominis. Participants will undergo non-invasive assessment of spinal curvature for comparison purposes. No intervention will be administered. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Lumbar Lordosis Angle
Lumbar lordosis angle measured in degrees in postpartum women with and without diastasis recti abdominis using a non-invasive assessment method.
Measured: At baseline (single assessment).
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Mar 2026
- Study start2 Mar 2026 (estimated)
- Primary completion20 Apr 2026 (estimated)
- Study completion27 Apr 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Diastasis Recti AbdominisStudies of the same condition, open and under way.
- More trials run by Cairo UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Cross-sectional
- Enrolment
- 110 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Cairo University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Mawada Mohamed Ali Altemamy, Cairo University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07458412
- Sponsor's protocol ID
- 012\006165
- Acronym
- DRA-SC
- Status last verified
- Mar 2026
- First submitted
- 4 Mar 2026
- Last updated
- 9 Mar 2026
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 9 Mar 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Impact of Diastasis Recti Abdominis on Spinal Curvature in Postpartum Women
- ClinicalTrials.gov ID
- NCT07458412
- Acronym / sponsor ID
- DRA-SC / 012\006165
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 110 participants (estimated)
- Lead sponsor
- Cairo UniversityUniversity, hospital or other
- Study start
- 2 Mar 2026 (estimated)
- Primary completion
- 20 Apr 2026 (estimated)
- Study completion
- 27 Apr 2026 (estimated)
- First posted
- 9 Mar 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study investigates the relationship between diastasis recti abdominis and spinal curvature in postpartum women using non-invasive assessment methods.
Detailed description
Postpartum musculoskeletal changes are common and may significantly affect spinal alignment and overall physical function. Diastasis recti abdominis (DRA), a separation of the abdominal muscles after pregnancy, is frequently reported among postpartum women and may contribute to alterations in trunk stability and posture. Despite its high prevalence, the potential association between DRA and spinal curvature has not been sufficiently clarified. Understanding this relationship is important, as changes in spinal alignment-such as increased lumbar lordosis or thoracic kyphosis-may influence pain, functional ability, and long-term musculoskeletal health. Therefore, further investigation is needed to better define the connection between DRA and spinal curvature in order to support early assessment and improve postpartum rehabilitation strategies.
Study design
- Observational model
- Other
- Time perspective
- Cross-sectional
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Women with Diastasis Recti | – | –Postpartum women diagnosed with diastasis recti abdominis. Participants will undergo non-invasive assessment of spinal curvature for comparison purposes. No intervention will be administered. |
| Women without Diastasis Recti | – | –Postpartum women without diastasis recti abdominis. Participants will undergo non-invasive assessment of spinal curvature for comparison purposes. No intervention will be administered. |
Who may qualify
- Ages
- 21 to 35 years
- Sex
- Female only
- Age groups
- Adult
- Study population
- The study population will include postpartum women who meet the eligibility criteria. Participants will be divided into two groups based on the presence or absence of diastasis recti abdominis and will undergo non-invasive assessment of spinal curvature for comparative analysis.
Key inclusion criteria (5 listed)
- Age range: 21 to 35 years
- BMI between 18 and 29.9 kg/m².
- Normal vaginal delivery or cesarean section.
- Postpartum period between 6 weeks and 6 months
- Participants with or without diastasis recti abdominis (DRA) as determined by ultrasound.
Key exclusion criteria (6 listed)
- • History of spinal deformities (e.g., scoliosis, kyphosis, spondylolisthesis).
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Lumbar Lordosis Angle
Time frame: At baseline (single assessment).
Lumbar lordosis angle measured in degrees in postpartum women with and without diastasis recti abdominis using a non-invasive assessment method.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 9 Mar 2026.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Questions about this trial
What is this clinical trial studying?
An observational study of Diastasis Recti Abdominis and Lumbar Lordosis, run by Cairo University.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 9 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Mawada Mohamed, Master (+01027877397, mawadamohamed45@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Lumbar Lordosis Angle (time frame: At baseline (single assessment).). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Mar 2026.