ClinicalTrials.Veeva

Menu

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

S

Superior University

Status

Unknown

Conditions

Stroke

Treatments

Diagnostic Test: PNF
Diagnostic Test: TRT

Study type

Interventional

Funder types

Other

Identifiers

NCT05391009
DPT/Batch-Fall17/513

Details and patient eligibility

About

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

Full 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.

Enrollment

52 estimated patients

Sex

All

Ages

50 to 70 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

52 participants in 2 patient groups

PNF GROUP
Experimental group
Description:
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
Treatment:
Diagnostic Test: PNF
TRT GROUP
Experimental group
Description:
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.
Treatment:
Diagnostic Test: TRT

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems