PNF Strengthening and De-lorme and Watkins Exercises on Upper Extremity Function and Strength in Stroke Patients

Sponsor
Riphah International University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05904795
Collaborator
(none)
20
1
2
8.1
2.5

Study Details

Study Description

Brief Summary

The aim of this study is to evaluate the effects of proprioceptive neuromuscular facilitation strengthening exercises and de-Lorme and Watkins exercises program in stroke patients with upper limb weakness in chronic stroke patients. The randomized central trial will recruit patients according to consecutive sampling into two intervention groups. One group will receive proprioceptive neuromuscular facilitation strengthening exercises and other group will receive de-Lorme and Watkins exercises program.

Condition or Disease Intervention/Treatment Phase
  • Other: PNF strengthening exercises
  • Other: de-lorme and watkins exercises
N/A

Detailed Description

A study in which the participants (n=26) were recruited in the study suffering from stroke and meeting the inclusion criteria. Two groups formed such that patients in group A will be treated with conventional therapy and PNF and group B will be treated with PNF and NMES in along with conventional therapy. The protocol will cover 6 weeks of treatment. Regular assessment at 0,3rd and 6th week will be carried out. In the rehabilitation period, we will evaluate upper extremity function, activities of daily living(ADLs), mental status examination at regular interval during the rehabilitation.In previous studies there is less literature regarding the combine effects of proprioceptive neuromuscular facilitation techniques and de-Lorme and Watkins exercise program on upper limb function and strength in chronic stroke patients with upper limb weakness. Therefore there is dire need to explore which training technique is most effective in improving upper limb function and strength in chronic stroke patients therefore this study aims in comparative effects of proprioceptive neuromuscular facilitation strengthening exercises and de-Lorme and Watkins exercise program on upper limb function and strength in chronic stroke patients.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
Comparative Effects of Proprioceptive Neuromuscular Facilitation Strengthening Exercises and De-lorme and Watkins Exercises Program on Upper Limb Function and Strength in Chronic Stroke Patients
Actual Study Start Date :
Feb 25, 2023
Anticipated Primary Completion Date :
Oct 18, 2023
Anticipated Study Completion Date :
Oct 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: PNF strengthening exercises

Pnf strengthening exercises along with isometrics and range of motion exercises

Other: PNF strengthening exercises
PNF strengthening exercises 10 repetitions, 1set , 4 days/week along with range of motion exercises total of 4 sessions were given consisting 40 minutes

Active Comparator: de-lorme and watkins progressive resistance exercises

progressive resistance exercises along with isometrics and range of motion exercises

Other: de-lorme and watkins exercises
The group was given de-lorme and watkins progressive resistance exercises along with range of motion exercises .10 repetitions, 1set, 4 days /week along with range of motion exercises. total of 4 sessions per week each consisting of 40 minutes.

Outcome Measures

Primary Outcome Measures

  1. The barthel index scale [4th day]

    The Barthel Index (BI) is a measure of independence in activities of daily living (ADL).It contains 10 components which has different scores.The total score is calculated by dividing 100.

  2. Hand held dynamometer [4th day]

    The hand held dynamometry is an objective method in detecting minimum muscle strength change, which has an impact on the physical function of ICU survivors. The minimum change in the fore can be measured in units of weight such as pounds or kilograms.

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Chronic stroke patients.

  • Medically stable patients having a single stroke.

  • History of stroke 6 to 24 months.

  • A score greater than 24-30 in mini-mental test.

  • Patients having consciousness with GC;10

Exclusion Criteria:
  • Recurrent stroke

  • Patients with gullian berrie syndrome, multiple sclerosis lesion osteoarthritis of shoulder.

  • Manual muscle testing below grade II.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Shahida Islam teaching hospital Lodhran Lodhran Punjab Pakistan 47541

Sponsors and Collaborators

  • Riphah International University

Investigators

  • Principal Investigator: Hira Jabeen, MSNMPT, Riphah International Universiry

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Riphah International University
ClinicalTrials.gov Identifier:
NCT05904795
Other Study ID Numbers:
  • REC/LHR/23/0215 ZAINAB TEHREEM
First Posted:
Jun 15, 2023
Last Update Posted:
Jun 15, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Riphah International University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 15, 2023