- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07506174
Pelvic PNF and Multiplanar Trunk Training in Stroke Patients
Comparative Effects of Pelvic Proprioceptive Neuromuscular Facilitation and Multiplanar Trunk Training on Balance and Functional Mobility in Stroke Patients
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Muneeb khan, PhD
- Phone Number: +92336799611
- Email: muneeb.khan@riphah.edu.pk
Study Locations
-
-
Punjab Province
-
Lahore, Punjab Province, Pakistan, 54500
- Al-e-Imran Trust Hospital
-
Contact:
- Sana Riaz, MS
- Phone Number: +923474716107
-
Principal Investigator:
- Saba Naseem Khan, MsNMPT
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Chronic Hemiplegia, at least six months after the first stroke episode, stroke victims go through a recovery phase
- Ischemic and Hemorrhagic stroke
- Patients who can sit independently
- Patient with a Standardized Mini-Mental State Examination (SMMSE) score ≥ 24
- Patient with the ability to walk 10 meters independently using aids or orthosis
Exclusion Criteria:
- patients who had any form of spine or lower limb surgery within the past month
- Patients with unstable cardiovascular disorders
- Patients with other neurological or musculoskeletal disorders that resulted in significant balance issues, such as basal ganglia or cerebellar disorders
- Patients with fractures and dislocations in the spine and lower limbs
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 |
|---|---|
|
Active Comparator: Pelvic Proprioceptive Exercises
|
Pelvic Anterior Elevation Pelvic Posterior Elevation Pelvic Anterior Depression Pelvic Posterior Depression 5 reps of every exercise, 30 minutes for 12 weeks |
|
Experimental: Multiplanar Trunk Training
|
Sitting Balance on a Stable Surface Static Trunk Holds with Supportive Surfaces Static Trunk Rotation Seated Trunk Rotation (Right and Left) Seated Lateral Flexion (Right and Left) Seated Anterior-Posterior Weight Shifting Seated Trunk Rotations with Arm Reaching Bridging with Arm Reaches Wall Push-ups Ball Tossing or Catching in Sitting/Standing 5-7 reps of every exercise for 30 minutes for 12 weeks |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Berg Balance Scale (BBS)
Time Frame: 12th week
|
The BBS comprises 14 items specifically designed to evaluate balance function in older adults.
Each item is assigned a score on a 5-point scale ranging from 0 to 4. The cumulative score ranges from 0 to 56, with a higher score indicating superior balance function.
|
12th week
|
|
Timed Up and Go Test (TUG)
Time Frame: 12th week
|
In the timed up and go (TUG) test, subjects are asked to rise from a standard armchair, walk to a marker 3 m away, turn, walk back, and sit down again.
The TUG test is used to assess dynamic balance, mobility, and the risk of falls.
The task consists of getting up from a chair, walking 3 m, turning around, returning to the chair, and sitting down.
The test will be repeated 3 times.
|
12th week
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sana Riaz, MS, Riphah International University
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR & AHS/24/02107
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.
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