Actively Recruiting
Effects of Stabilizing Reversal and Rhythmic Stabilization Versus Pelvic Proprioceptive Neuromuscular Facilitation on Trunk Control, Postural Stability, and Mobility in Stroke Patients
Led by Riphah International University · Updated on 2024-12-27
50
Participants Needed
1
Research Sites
35 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating the effects of two different physical therapy techniques—stabilizing reversal and rhythmic stabilization versus pelvic proprioceptive neuromuscular facilitation—on trunk control, postural stability, and mobility in patients who have experienced an ischemic stroke. This randomized clinical trial includes 50 participants aged 40 to 65 years who have had a stroke within the last six months and can understand simple verbal commands. The study aims to determine if there is a difference in how these treatments affect key physical functions in stroke recovery. Participants will be randomly assigned to one of two groups. Group A will undergo stabilizing reversals and rhythmic stabilization exercises, performing 3 sets of 15 repetitions per session, five days a week for eight weeks. Group B will receive pelvic proprioceptive neuromuscular facilitation treatments, also five days a week for eight weeks, with each session lasting 30 minutes. Both treatment protocols span a total of 40 sessions. Throughout the study, participants will be evaluated at the start, mid-point (4 weeks), and end (8 weeks) using several tests: the Trunk Impairment Scale for trunk control, the Postural Assessment Scale and Functional Reach Test for postural stability, and the Performance Oriented Mobility Assessment for mobility. Researchers will monitor and analyze changes over time to assess the effectiveness of each intervention, using appropriate statistical methods to compare results between and within groups.
CONDITIONS
Official Title
Stabilizing Reversal and Rhythmic Stabilization vs Pelvic Proprioceptive Neuromuscular Facilitation in Stroke Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed cases of ischemic stroke.
- Both genders of stroke patients.
- Age of stroke patients between 40-65 years.
- Duration of stroke less than 6 months.
- Participants should be able to understand and follow simple verbal commands (MMSE 24).
You will not qualify if you...
- Recurrent history of stroke.
- Recent history of any trauma.
- Musculoskeletal disorders such as low back pain, arthritis, degenerative diseases of the lower limbs affecting motor performance, spinal deformity and contractures.
- Spasticity (modified Ashworth scale grade 653) or flaccidity in lower limbs and upper limbs.
- PNF treatment given to the pelvic region within 6 weeks.
AI-Screening
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Trial Site Locations
Total: 1 location
1
Lahore General Hospital
Lahore, Punjab Province, Pakistan, 54600
Actively Recruiting
Research Team
I
Imran Amjad, Phd
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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