Effects of TENS With and Without Core Stabilization Exercises on Low Back Pain, Inter-Recti Distance, and Transversus Abdominis Thickness in Postpartum Women With Diastasis Recti Abdominis
NCT07929727, Not applicable, Active not recruiting, University of Management and Technology Lahore
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Effects of TENS With and Without Core Stabilization Exercises on Low Back Pain, Inter-Recti Distance, and Transversus Abdominis Thickness in Postpartum Women With Diastasis Recti Abdominis | ClinicalTrials.gov |
| NCT number | NCT07929727 | ClinicalTrials.gov |
| Status | Active not recruiting | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 36 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | University of Management and Technology Lahore | ClinicalTrials.gov |
| Conditions | Diastasis Recti Abdominis (Postpartum) | ClinicalTrials.gov |
| Interventions | Transcutaneous Electrical Nerve Stimulation (TENS) alone., TENS combined with Core Stabilization Exercises | ClinicalTrials.gov |
| First posted | 2026-11-10 | ClinicalTrials.gov |
| Last updated | 2026-11-10 | ClinicalTrials.gov |
Registered outcomes 3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | DIGITAL VERNIER CALIPER | baseline and after 6 weeks | A Digital Vernier Caliper is a precision measuring instrument used to measure linear distances accurately. In patients with Diastasis Recti Abdominis (DRA), it can be used to assess the Inter-Recti Distance (IRD), which is the separation between the two rectus abdominis muscles. The device provides measurements in millimeters (mm) and offers high accuracy and reliability for clinical assessment. | ClinicalTrials.gov |
| Primary | MSK ULTRASOUND | baseline and after 6 weeks | Musculoskeletal Ultrasound (MSK-US) is a real-time, non-invasive imaging tool used to measure the thickness and activation of the Transversus Abdominis (TrA), especially in postpartum females with Diastasis Recti. | ClinicalTrials.gov |
| Primary | OSWESTRY DISABILITY INDEX | baseline and after 6 weeks | The Oswestry Disability Index (also known as the Oswestry Low Back Pain Disability Questionnaire) is an extremely important tool that researchers and disability evaluators use to measure a patient's permanent functional disability. The test is considered the "gold standard" of low back functional outcome tools. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
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Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Grants 0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)