NCT07609407 Effect of Pelvic Stability Training on Lower Limb Motor Function in Subacute Stroke
| NCT ID | NCT07609407 |
| Status | Recruiting |
| Phase | — |
| Sponsor | University of Faisalabad |
| Condition | Stroke |
| Study Type | INTERVENTIONAL |
| Enrollment | 34 participants |
| Start Date | 2026-05-19 |
| Primary Completion | 2026-07-18 |
Eligibility & Interventions
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 34 participants in total. It began in 2026-05-19 with a primary completion date of 2026-07-18.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
A stroke occurs when blood stops flowing through a blood vessel to the brain, typically from a burst blood vessel or a blood clot. Hemiparesis is associated with impairment of motor function in the lower limb(s) and with instability of the pelvis. The purpose of this study is to investigate the impact of pelvic stability training on the lower limb motor function after subacute stroke. A randomized clinical trial was conducted with 34 participants (17 in each group). This study will utilize the Non-Probability sampling technique called Consecutive sampling technique. All participants are included/excluded based on the inclusion and exclusion criteria and have signed informed consent (both written and verbal). Participants will be block randomized in to two group, one will get pelvic stability training and lower limb passive stretching and lower limb NMES (Neuromuscular electrical stimulation) and other group will get only lower limb passive stretching and lower limb NMES. Both interventions will be administer over a Eight- week period, thrice a week (alternative days). The results of the study will be pelvic tilt, fugal-meyer assessment lower extremities and cadence of gait. Data will be gathered at baseline and following the 8 week session. Data will be analysed by SPSS 23 program.
Eligibility Criteria
Inclusion Criteria: * Age: 40-60 years * Gender: both Male and Female. * 1st episodes of stroke either haemorrhagic and Ischemic * Standing Ability with or without assistance aid/mobility Beyond burnstorm stage 3,argue that Burnstrom stage beyond 3 will be recruited. Exclusion Criteria: * Neurological and musculoskeletal dysfunction Any past history of Fracture of the lower limb/ pelvis • Any Implant Cardiac pathology
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07609407 clinical trial?
This trial is open to participants of all sexes, aged 40 Years or older, up to 60 Years, studying Stroke. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07609407 currently recruiting?
Yes, NCT07609407 is actively recruiting participants. Contact the research team at liezaiftikhar.dpt@tuf.edu.pk for enrollment information.
Where is the NCT07609407 trial being conducted?
This trial is being conducted at Faisalabad, Pakistan.
Who is sponsoring the NCT07609407 clinical trial?
NCT07609407 is sponsored by University of Faisalabad. The trial plans to enroll 34 participants.
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