Effects of PNF on Shoulder Pain in Paraplegic Manual Wheel Chair Users

Sponsor
Riphah International University (Other)
Overall Status
Completed
CT.gov ID
NCT04967911
Collaborator
(none)
22
1
2
7
3.2

Study Details

Study Description

Brief Summary

This project was a Randomized control trial conducted to check the Effects of Proprioceptive Neuromuscular Facilitation on Shoulder Pain due to chronic impingement syndrome in paraplegic Manual Wheelchair users after Spinal Cord Injury so that we can have best treatment option for patients with shoulder pain due to manual wheelchair usage. duration was of 6months,convenient sampling was done, subject following eligibility criteria from Spine welfare trust center, Nawaz Sharif social security Hospital were randomly allocated in two groups via lottery method, Group A participants were given baseline treatment along with PNF exercises , Group B participants were given baseline treatment upto 6 weeks and 3 sessions per, post intervention assessment was done after 6 weeks, by self-generated questionnaire (WUSPI) wheel chair users shoulder pain index, (SRQ) Shoulder rating questionnaire and physical assessment by 2 special test was done, data was analyzed by using SPSS version 25.

Condition or Disease Intervention/Treatment Phase
  • Other: Rhythmic stabilization exercises
  • Other: conventional treatment
N/A

Detailed Description

In paraplegic manual wheelchair users Shoulder pain is most common problem after spinal cord injury. Due to wheelchair propulsion, weight relief task and other household activities repetitive load induced on upper limb and put substantial load in particular on shoulder.In spinal cord injured patients shoulder pain is because of over use of upper limb and shoulder during wheelchair related activities and personal care activities. less stability and slight muscle mass leads toward pain in their life at some point because of Muscular imbalance and later on shoulder secondary impingement syndrome. This study compared the rhythmic stabilization technique from PNF exercises with conventional treatment on experimental and control group to see the difference in reduction of pain and disability.

Study Design

Study Type:
Interventional
Actual Enrollment :
22 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Effects of Propioceptive Neuromuscular Facilitation Technique on Shoulder Pain in Paraplegic Manual Wheel Chair Users After Spinal Cord Injury
Actual Study Start Date :
Nov 30, 2020
Actual Primary Completion Date :
May 30, 2021
Actual Study Completion Date :
Jun 30, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Rhythmic stabilization exercises

baseline physical therapy conventional treatment along Rhythmic stabilization exercises

Other: Rhythmic stabilization exercises
PNF techniques and Conventional Treatment: Experimental group received rhythmical Stabilization Technique on shoulder joint on all shoulder movements up to 1 minute in supine position For stability of joint ,re-establish dynamic rotator cuff stability and to enhance MS strength and decrease pain. Conventional Treatment: heating pad for 15 minutes, TENS (Transcutaneous Electrical Nerve Stimulation) and after that shoulder stretching of upper trapezius muscle, pectorals and levator scapule and isometric exercises of rotator cuff muscles performed in supine .( 10 sec hold and 10 to 15 reps)..

Other: Conventional treatment

Baseline physical therapy conventional treatment

Other: conventional treatment
Conventional Treatment: heating pad for 15 minutes, TENS (Transcutaneous Electrical Nerve Stimulation) and after that shoulder stretching of upper trapezius muscle, pectorals and levator scapule and isometric exercises of rotator cuff muscles performed in supine .( 10 sec hold and 10 to 15 reps)..

Outcome Measures

Primary Outcome Measures

  1. Wheelchair User's Shoulder Pain Index [6th Week]

    The Wheelchair User's Shoulder Pain Index (WUSPI) was designed to measure shoulder pain in individuals who use wheelchairs. On the visual analog scale from ' 0' to '10 ' estimate level of pain with different activities

Secondary Outcome Measures

  1. Shoulder rating Questionnaire [6th Week]

    Shoulder rating questionnaire (SRQ) was designed to assess the severity of symptoms related to and the functional status of the shoulder. It includes domains of global assessment, pain, daily activities, recreational and athletic activities, work, satisfaction, and areas for improvement. Each domain is graded separately and is weighted to arrive at the total score

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 18-60 years old paraplegic manual wheel chair users after spinal cord injury.

  • Those having level of injury from C7-T12

  • Patients who are using wheelchair from more than one year.

  • Pain perceived region of one or both Shoulder from last three months or more

  • Pain without radicular symptoms radiating to whole upper limbs.

  • Wheelchair propulsion in activities of daily living,

  • Individuals with positive Neer's test and Hawkins-Kennedy test

Exclusion Criteria:
  • Any red flags (tumor, fracture, metabolic diseases, rheumatoid arthritis, resting blood pressure greater than 140/90 mmHg, prolonged history of steroid use, etc.

  • Any dislocation ,muscular tear and acute problem of shoulder.

  • Presented with a diagnosis of cervical spinal stenosis, exhibited bilateral upper extremity symptoms

  • Any recent surgery of the shoulder

  • Individuals using other mobility devices with wheelchair.

  • Individuals with primary impingement

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mansoora hospital, Lahore, Spine welfare centre, Social security hosital Lahore Punjab Pakistan

Sponsors and Collaborators

  • Riphah International University

Investigators

  • Principal Investigator: Mehwish Ikram, MS, Riphah International University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Riphah International University
ClinicalTrials.gov Identifier:
NCT04967911
Other Study ID Numbers:
  • REC/Lhr/21/0205 Hira
First Posted:
Jul 20, 2021
Last Update Posted:
Jul 20, 2021
Last Verified:
Jul 1, 2021
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 Jul 20, 2021