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Clinical Trials/NCT03161782
NCT03161782
Completed
Not Applicable

The Efficacy of Proprioceptive Neuromuscular Facilitation Stretching and Static Stretching on Range of Motion, Pain and Function in Elbow Limitation

Istanbul University1 site in 1 country40 target enrollmentJanuary 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative Pain
Sponsor
Istanbul University
Enrollment
40
Locations
1
Primary Endpoint
Functional Status
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The aim of the study is to compare the efficacy of Proprioceptive Neuromuscular Facilitation (PNF) stretching and static stretching on range of motion (ROM), pain and function in elbow limitation.

Detailed Description

To compare the efficacy of PNF stretching and static stretching on ROM, pain and function in elbow limitation, forty voluntary patients with elbow limitation, aged between 18-55 years will be randomly divided into two groups: PNF Stretching group and Static Stretching group. PNF stretching will be combined with exercise and cold application in PNF Stretching group, static stretching will be combined with exercise and cold application in Static Stretching group, will be applied for 12 sessions. The patients will be assessed before and after six-week treatment. The pain on activity, at rest and at night will be assessed with Visual Analog Scale (VAS). ROM will be assesed with universal goniometer. The functional status will be evaluated by Disabilities Arm, Shoulder and Hand (DASH). Kinesiophobia and quality of life will be assessed with Tampa Scale for Kinesiophobia and Short Form-12, respectively. The Global Rating of Change will be used to evaluate patient satisfaction.

Registry
clinicaltrials.gov
Start Date
January 1, 2017
End Date
July 25, 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Tansu Birinci

Research Assistant

Istanbul University

Eligibility Criteria

Inclusion Criteria

  • Subjectswill be included with
  • Aged between 18 and 65 years
  • Elbow fracture in the six months before the study
  • Elbow limitation in flexion or extension
  • Being volunteer to participate
  • Fractures should be managed with conservatively or surgically

Exclusion Criteria

  • Malunion or Nonunion Fracture
  • Occurrence of complex regional pain syndrome, peripheric nerve injury, heterotopic ossification, myositis ossification or post-traumatic ankylosing
  • Non-healing wound or infection
  • Previously received physiotherapy for elbow limitation
  • Having any cardiovascular diseases, neurological disorders, rheumatic diseases or psychiatric diseases
  • Could not adjust to treatment

Outcomes

Primary Outcomes

Functional Status

Time Frame: After the six-week intervention

The functional status of the patients will be evaluated by The Disabilities of the Arm, Shoulder and Hand (DASH).

Secondary Outcomes

  • Active Range of Motion (AROM) Assessment(1-month follow up)
  • Functional Status(1-month follow up)
  • Pain Intensity(1-month follow up)

Study Sites (1)

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