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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05391009
Other study ID # DPT/Batch-Fall17/513
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date March 31, 2022
Est. completion date September 2022

Study information

Verified date May 2022
Source Superior University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Comparison of PNF and Task Related Techniques Along with Tens on Upper Limb Function Among Stroke Patients


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.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 52
Est. completion date September 2022
Est. primary completion date June 2022
Accepts healthy volunteers No
Gender All
Age group 50 Years to 70 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
PNF
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
TRT
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.

Locations

Country Name City State
Pakistan General hospital, Al Shafi hospital, CH. Muhammad Akram Hospital Hameed Latif Hospital. Lahore

Sponsors (1)

Lead Sponsor Collaborator
Superior University

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Task Related Techniques Along With Tens on Upper Limb Function Among Stroke Patients 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 PNF Techniques Along With Tens on Upper Limb Function Among Stroke Patients 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
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