- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05391009
Comparison of PNF and Task Related Techniques Along With Tens on Upper Limb Function Among Stroke Patients
May 22, 2022 updated by: Muhammad Naveed Babur, Superior University
Comparison of PNF and Task Related Techniques Along with Tens on Upper Limb Function Among Stroke Patients
Study Overview
Status
Enrolling by invitation
Conditions
Intervention / Treatment
Detailed Description
The objective of this study is to determine the comparison of PNF and TRT along with TENs on upper limb function recovery among stroke patients.
Study Type
Interventional
Enrollment (Anticipated)
52
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Lahore, Pakistan
- General hospital, Al Shafi hospital, CH. Muhammad Akram Hospital Hameed Latif Hospital.
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
50 years to 70 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Duration of illness before participation in the study ranged from six to eighteen months' post stroke.
- Patients who diagnosed with ischemic stroke stage 2 and 3
- Patients' age ranged from 50-70 years (male/female)
- Patients with sufficient cognitive abilities that enables them to understand and follow instructions (mini mental scale)
Exclusion Criteria:
- Patients with communication problems
- Patients with a history of previous stroke or other neurological diseases or disorders
- Patients with inflammation, old fracture or prosthesis in the affected limb, neurological diseases that affect upper limb function other than stroke (e.g.: Multiple sclerosis, Peripheral neuropathy, Parkinsonism .... etc.), infection or dermatological conditions on acupuncture sites, musculoskeletal disorders such as severe arthritis, cardiovascular problems (unstable angina, recent myocardial infarction within the last three months, congestive heart failure, significant heart valve dysfunction, arrhythmia, implanted pacemaker or unstable hypertension) or pulmonary disorders, visual and auditory problems and patients with cognitive impairment.
- Any Contra indications for TENS, Other neurological & orthopedic conditions affecting upper limb, Patient with subluxed shoulder, Patient with shoulder hand syndrome.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: PNF GROUP
PNF exercise twice daily five days per week for 8 weeks.
D1 and D2 flexion and extension pattern for upper limb.
In D1 Flexion-adduction -external rotation d1, extension -abduction-internal rotation and in D2 flexion-abduction-external rotation, extension-adduction-internal rotation
|
PNF exercise twice daily five days per week for 8 weeks.
D1 and D2 flexion and extension pattern for upper limb.
In D1 Flexion-adduction -external rotation d1, extension -abduction-internal rotation and in D2 flexion-abduction-external rotation, extension-adduction-internal rotation
|
|
Experimental: TRT GROUP
The duration of a TRT session Will be 60 min.
Each session started with warm-up exercises for 10 min followed by 50 min of TRT.
Each task will be repeated approximately 10 to 20 times, for 1 to 5 sets, or alternatively for 2 to 5 min.
A 2 min rest period after every 15 min of practice will be allowed.
Before commencing the exercise session, tasks will be demonstrated to each patient using the non-affected UE.
|
The duration of a TRT session Will be 60 min.
Each session started with warm-up exercises for 10 min followed by 50 min of TRT.
Each task will be repeated approximately 10 to 20 times, for 1 to 5 sets, or alternatively for 2 to 5 min.
A 2 min rest period after every 15 min of practice will be allowed.
Before commencing the exercise session, tasks will be demonstrated to each patient using the non-affected UE.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Task Related Techniques Along With Tens on Upper Limb Function Among Stroke Patients
Time Frame: 6 Months
|
The duration of a TRT session Will be 60 min.
Each session started with warm-up exercises for 10 min followed by 50 min of TRT.
Modified ashworth scale (mas) Box and block test
|
6 Months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
PNF Techniques Along With Tens on Upper Limb Function Among Stroke Patients
Time Frame: 6 Months
|
PNF exercise twice daily five days per week for 8 weeks.
D1 and D2 flexion and extension pattern for upper limb.
Mini Mental Scale
|
6 Months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 31, 2022
Primary Completion (Anticipated)
June 1, 2022
Study Completion (Anticipated)
September 1, 2022
Study Registration Dates
First Submitted
May 9, 2022
First Submitted That Met QC Criteria
May 22, 2022
First Posted (Actual)
May 25, 2022
Study Record Updates
Last Update Posted (Actual)
May 25, 2022
Last Update Submitted That Met QC Criteria
May 22, 2022
Last Verified
May 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- DPT/Batch-Fall17/513
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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