Trial · NCT07889791
Effects Of Core Canister Training in Pregnant Women With History of Gestational Diabetes Mellitus
NCT07889791, Not applicable, Recruiting, University of Lahore
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effects Of Core Canister Training in Pregnant Women With History of Gestational Diabetes Mellitus. Trials, record NCT07889791. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07889791
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effects Of Core Canister Training in Pregnant Women With History of Gestational Diabetes Mellitus
- NCT number
- NCT07889791
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 90 participants, estimated
- Lead sponsor
- University of Lahore
- Conditions
- Antenatal Care Model, Gestatiaonl Diabetes Mellitus
- Interventions
- core canister training, traditional antenatal exercises
- First posted
- 2026-10-22
- Last updated
- 2026-10-22
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Musculoskeletal Ultrasound Imaging | 12th week | is a non-invasive, real-time imaging technique used to quantify muscle thickness and activation widely used in clinical and research settings. Studies consistently show excellent within-examiner reliability (ICC ≥ 0.90) for core muscle thickness measurements across different muscles |
| Primary | Modified oxford scale | 12th week | A 6-point digital vaginal palpation scale (0-5) used to grade voluntary pelvic floor muscle strength in women. Correlation coefficients reported between r = 0.60-0.80, Indicates moderate to strong correlation with instrumented measures and intra-rater Reliability is generally good to excellent (ICC range: \~0.80-0.95). |
| Primary | Active Straight Leg Raise (ASLR) Test | 12th week | The Active Straight Leg Raise (ASLR) Test is a functional clinical test used to assess ability to generate and transfer load/motor control across the lumbopelvic region, particularly in patients with pelvic girdle pain and suspected instability. Test-Retest Reliability is good to excellent (ICC ≈ 0.83 and Pearson's r ≈ 0.87) |
| Primary | Y-Balance Test (YBT) | 12th week | The Y-Balance Test (YBT) is a clinical dynamic balance and functional stability test derived from the Star Excursion Balance Test that assesses a person's ability to maintain balance and control while reaching in three directions (anterior, posteromedial, posterolateral) on a single stance leg - reflecting aspects of lumbopelvic motor control and dynamic stability. Excellent inter-rater reliability has been reported: ICC ≈ 0.99-1.00 for reach distances and composite scores in young adults with chronic low back pain |
| Primary | International Consultation on Incontinence Questionnaire - Urinary Incontinence Short Form (ICIQ-UI SF) | 12th week | A short, self-reported questionnaire (3 scored items + 1 unscored) that assesses frequency, severity, and impact of urinary incontinence on quality of life. Widely used in clinical and research settings, including pregnancy and postpartum women. Reliability: Excellent test-retest reliability with ICC = 0.95. Validity: Strong construct validity, correlating well with bladder diaries and pad tests (r = 0.72-0.89). Good internal consistency: Cronbach's α = 0.91 |
| Primary | King's Health Questionnaire (KHQ) | 12th week | A condition-specific, self-administered quality-of-life questionnaire for urinary incontinence (UI). It consists of 21 items in 9 domains (e.g., general health, incontinence impact, role/emotional/physical/social limitations, sleep/energy, severity measures, and personal relationships). Reliability: High internal consistency: Cronbach's α = 0.72-0.97 across domains. Excellent test-retest reliability: ICC = 0.79-0.93. Validity: (correlation coefficients r = 0.60-0.80). |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers8
The papers the trial lists on ClinicalTrials.gov.
Grants0
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.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.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.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07889791
GET https://conductscience.org/api/trials/v1/NCT07889791/registered