ClinicalTrials.gg
Enrolling by invitationNCT07560774Updated Oct 26, 2026

Online-Delivered Core Stability Exercises in Postpartum Women

An interventional study of online core stability exercise group and an education-only control group in Postpartum, Trunk Muscle Endurance and Postural Stability, sponsored by Prince Sattam Bin Abdulaziz University. Enrolling by invitation at 1 site in Saudi Arabia. Open to female participants aged 20 Years to 40 Years. Per ClinicalTrials.gov, last updated 2026-10-26.

Sponsored by Prince Sattam Bin Abdulaziz University · Not applicable, Interventional, and Treatment

Updated Oct 21, 2026Now Enrolling by invitationFirst site in Saudi Arabia+1 moreGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
20 Years to 40 Years
Sex
Female
01

Study summary

This study will examine a 12-week online core stability program for postpartum women, where participants will complete supervised sessions three times per week and will be compared with an education-only group. The intervention group will participate in supervised, real-time sessions via a video-conferencing platform, three times per week for 12 weeks. Exercises combine isometric and dynamic core stability tasks, progressing in difficulty over time. Dynamic postural control will be assessed using the lower quarter Y-Balance Test (YBT-LQ), while trunk endurance will be measured using the flexor endurance, extensor endurance, and side bridge tests.

02

Conditions studied

  • Postpartum
  • Trunk Muscle Endurance
  • Postural Stability
03

In context

Lead sponsor

Prince Sattam Bin Abdulaziz University is the lead sponsor of 35 studies on the registry; 9 are open to participants now.

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

04

Who can participate

Ages eligible
20 Years to 40 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. singleton pregnancy;
  2. medically uncomplicated delivery;
  3. clearance from a healthcare provider to participate in low- to moderate-intensity exercise;
  4. self-reported difficulties with trunk endurance, balance, or early fatigue during daily activities.

Exclusion criteria

Exclusion Criteria:

  1. unresolved obstetric complications;
  2. 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.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
40 participants (estimated)

Study arms

  • 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.

    Other: online core stability exercise group

  • 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.

    Other: an education-only control group

Interventions

  • Otheronline core stability exercise group

    The intervention group participated in supervised, real-time sessions via a video-conferencing platform, three times per week for 12 weeks.

  • Otheran education-only control group

    Participants in the control group received standard postpartum education delivered online once every two weeks over the 12-week period.

06

What researchers measure

Primary outcomes

  1. Dynamic Postural Control

    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.

    Time frame: 12 weeks

  2. Trunk endurance

    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.

    Time frame: 12 weeks

07

Study locations

1 site
  • Prince Sattam Bin Abdelaziz University
    Riyadh, 002, Saudi Arabia
08

References and documents

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

Individual participant data

Plan to share: Undecided

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jun 2026 (actual). Primary completion is estimated for Dec 2026, 6 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Apr 21, 2026
First posted
May 1, 2026
StartActual
Jun 1, 2026
Primary completionEst.
Dec 1, 2026
CompletionEst.
Feb 1, 2027
Last update
Oct 26, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Status
Not yet recruiting→Enrolling by invitation
changed Oct 21, 2026
Sites
1 site added — first site in Saudi Arabia
Show site
  • Prince Sattam Bin Abdelaziz University · Riyadh, Saudi Arabia
Oct 21, 2026
Contact
No study contact listed any more: removed n•••@yahoo.com · •••8094
Oct 21, 2026
Show all 1 update
  1. Oct 21, 2026
    Not yet recruiting→Enrolling by invitation
    1 site added — first site in Saudi Arabia
    Show site
    • Prince Sattam Bin Abdelaziz University · Riyadh, Saudi Arabia
    Contact No study contact listed any more: removed n•••@yahoo.com · •••8094
    + 2 other changes: verification date and date precision

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07560774
Lead sponsor
Prince Sattam Bin Abdulaziz University
Responsible party
NADIA RADWAN (Principal investigator, Prince Sattam Bin Abdulaziz University) — Principal investigator
First posted
May 1, 2026
Start date
Jun 1, 2026
Primary completion
Dec 1, 2026 (estimated)
Completion
Feb 1, 2027 (estimated)
Last update
Oct 26, 2026

Oversight

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

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