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Recruiting NCT07609407

Effect of Pelvic Stability Training on Lower Limb Motor Function in Subacute Stroke

No phase Interventional Stroke

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: baseline treatment neuromuscular electrical stimulation and stretching exercises for lower limb and Pelvic Stability Training, Neuromuscular electrical stimulation and lower limb passive stretching.
Who it may be relevant to
Registry conditions: Stroke. Basic parameters: 40 years — 60 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Pakistan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

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.

Interventions

  • Procedure baseline treatment neuromuscular electrical stimulation and stretching exercises for lower limb and Pelvic Stability Training
    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).
  • Other Neuromuscular electrical stimulation and lower limb passive stretching
    Neuromuscular electrical stimulation and lower limb passive stretching

Primary outcome measures

  • fugal-meyer [Time frame: 8 weeks]
  • Pelvic tilt [Time frame: 8 weeks]
Secondary outcome measures (1)
  • cadence of gait. [Time frame: 8 weeks]

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Pakistan · 1 center
  • Madinah Teaching Hospital — Faisalabad

Identifiers

NCT: NCT07609407 · TUF/EIRB/171/26

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗