- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07560774
Online-Delivered Core Stability Exercises in Postpartum Women
Effects of Online-Delivered Core Stability Exercises on Postural Control and Trunk Endurance in Postpartum Women
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Nadia Radwan, PHD
- Phone Number: +966561728094
- Email: nadiaradwan18@yahoo.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- singleton pregnancy;
- medically uncomplicated delivery;
- clearance from a healthcare provider to participate in low- to moderate-intensity exercise;
- self-reported difficulties with trunk endurance, balance, or early fatigue during daily activities.
Exclusion Criteria:
- unresolved obstetric complications;
- severe pelvic floor dysfunction requiring specialized medical management; (3) neurological or musculoskeletal conditions affecting balance
(4) participation in structured core training more than once per week during the previous three months.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Online core stability exercise group
Participants in the intervention group will be engaged in an online-delivered core stability exercise program. Sessions will be conducted via a secure video-conferencing platform three times per week, with each session lasting 40-50 minutes. The exercise program will integrate both isometric and dynamic core stability tasks targeting the trunk flexors, extensors, lateral flexors, and hip musculature. Foundational exercises will include modified curl-up, bird-dog, side bridge, plank variations, and supine bridge. Dynamic components will incorporate controlled limb movements, diagonal patterns, and unstable support surfaces when appropriate. Exercise intensity and complexity will be progressively increased by adjusting lever length, base of support, repetition volume, and hold duration, while emphasizing proper breathing and pelvic floor engagement. |
The intervention group participated in supervised, real-time sessions via a video-conferencing platform, three times per week for 12 weeks.
|
|
Experimental: An education-only control group
Participants in the control group will receive standard postpartum education delivered online once every two weeks over the 12 weeks.
Education sessions will focus on general postpartum health, infant care, sleep hygiene, and psychological well-being, but will not include structured or supervised exercise.
Control participants will be advised to maintain their usual daily activities and will not be restricted from engaging in light, unsupervised physical activity as recommended by their healthcare providers.
|
Participants in the control group received standard postpartum education delivered online once every two weeks over the 12-week period.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dynamic Postural Control
Time Frame: 12 weeks
|
The lower quarter Y-Balance Test (YBT-LQ) will be used to assess dynamic postural control of the lower extremity.
Participants will perform maximal reach in the anterior, posteromedial, and posterolateral directions while maintaining single-leg stance on a standardized YBT device or equivalent setup.
Reach distances are normalized to leg length, and a composite score is calculated as the sum of the three directions divided by three times leg length, multiplied by 100.
|
12 weeks
|
|
Trunk endurance
Time Frame: 12 weeks
|
Trunk endurance will be evaluated using three standardized tests: (a) the flexor endurance test (time holding a seated trunk flexion position against gravity); (b) the extensor endurance test (time maintaining the torso in a horizontal position in prone with the pelvis supported); and (c) the side bridge test (time maintaining a side plank position on each side).
All endurance times will be recorded in seconds, with longer durations indicating better endurance.
|
12 weeks
|
Collaborators and Investigators
Publications and helpful links
General Publications
- Thabet, A.A.; Alshehri, M.A. Efficacy of deep core stability exercise program in postpartum women with diastasis recti abdominis: A randomised controlled trial. J. Musculoskelet. Neuronal Interact. 2019, 19, 62. 34. Stuge, B.; Lærum, E.; Kirkesola, G.; Vøllestad, N. The efficacy of a treatment program focusing on specific stabilizing exercises for pelvic girdle pain after pregnancy: A randomized controlled trial. Spine 2004, 29, 351-359. Wallace, J.; Raglin, J.; Jastremski, C. Twelve month adherence of adults who joined a fitness program with a spouse vs without a spouse. J. Sports Med. Phys. Fitness 1995, 35, 206-213. 41. Jarvis-Selinger, S.; Chan, E.; Payne, R.; Plohman, K.; Ho, K. Clinical telehealth across the disciplines: Lessons learned. Telemed. J. e-Health 2008, 14, 720-725. 42. Peng, X.; Su, Y.; Hu, Z.; Sun, X.; Li, X.; Dolansky, M.A.; Qu, M.; Hu, X. Home-based telehealth exercise training program in Chinese patients with heart failure: A randomized controlled trial. Medicine 2018, 97, e12069
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- RHPT/026/003
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Postpartum
-
Women and Infants Hospital of Rhode IslandNot yet recruitingPostpartum Anxiety | Paternal Postpartum Depression
-
Ege UniversityIzmir Bakircay UniversityCompletedPostpartum Care | Episiotomy Pain | Postpartum PainTurkey (Türkiye)
-
Women's College HospitalCanadian Institutes of Health Research (CIHR); Michael Garron HospitalCompletedPostpartum Depression | Postpartum Anxiety | Postpartum Blues | Postpartum Mood DisorderCanada
-
University Hospital, Clermont-FerrandUnknownPostpartum Depression | Postpartum Hemorrhage | Postpartum Women | Postpartum Stress | Postpartum AnxietyFrance
-
Northwestern UniversityRecruiting
-
University of PittsburghTuscarora Intermediate Unit 11Recruiting
-
University of Colorado, DenverEunice Kennedy Shriver National Institute of Child Health and Human Development...CompletedPostpartumUnited States, Guatemala
-
The Jones InstituteUnknownPostpartum Depressive Mood | Postpartum Sexual FunctionUnited States
-
Assistance Publique Hopitaux De MarseilleUnknown
Clinical Trials on online core stability exercise group
-
Ahi Evran University Education and Research HospitalCompleted
-
National Taiwan University HospitalCompletedNeuropathic Pain | Degenerative Lumbar DiseaseTaiwan
-
Ankara Yildirim Beyazıt UniversityCompleted
-
Cairo UniversityActive, not recruitingLow Bone Mineral Density | Down Syndrome (DS)Egypt
-
University of VirginiaCompleted
-
October 6 UniversityCompleted
-
Riphah International UniversityRecruiting
-
Burdur Mehmet Akif Ersoy UniversityNot yet recruitingManual Dexterity | Core Stability | Hand Grip Strength | Dental Students
-
Foundation University IslamabadCompletedMild Intermittent AsthmaPakistan