Istanbul University
Istanbul, Turkey (Türkiye)
NCT Number: NCT03161782
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.
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Notify Me18 year–65 year
All sexes
Interventional
Not applicable
Istanbul, Turkey (Türkiye)
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Subjectswill be included with
Exclusion criteria
For hold-relax stretching, each subject in PNF Stretching group will be comfortably positioned in a supine lying position, and patient will move the joint to the end of the passive or pain-free ROM. The therapist will ask for an isometric contraction of the restricting muscle or pattern (antagonists) with emphasis on rotation. The patients will be asked to perform submaximal isometric contractions of the target muscle for 10 seconds. After the contraction, the patients will be instructed to relax for 5 seconds. The joint will be repositioned actively to the new limit of range, and then therapist will passively control the new ROM. The procedure will be repeated 10 times with 10 seconds of rest between two successive trials. Patients will be treated 2 times per week for 6 weeks.
For static stretching, each subject in Static Stretching group will be comfortably positioned in a supine lying position, and the stretching of target muscle will be maintained for 20 seconds followed by 10 seconds of rest. The procedure will be repeated 10 times with 10 seconds of rest between two successive trials. Patients will be treated 2 times per week for 6 weeks.
Shoulder, elbow and wrist AROM exercises. Elbow flexion and extansion self-stretching exercises Elbow and wrist strengthening exercises Proprioception exercises for elbow. Grip strengthening exercises.
Cold therapy will be applied over the elbow for 15 minutes in the form of cold pack after stretching and exercise protocol.
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).
Time frame: Baseline
The elbow's and forearm's AROM, including flexion, extansion, supination, pronation will be measured described by the American Academy of Orthopaedic Surgeons (AAOS) using a universal goniometer. The process will be repeated three times in each direction, with the the average value recorded.
Time frame: After the six-week intervention
The elbow's and forearm's AROM, including flexion, extansion, supination, pronation will be measured described by the American Academy of Orthopaedic Surgeons (AAOS) using a universal goniometer. The process will be repeated three times in each direction, with the the average value recorded.
Time frame: 1-month follow up
The elbow's and forearm's AROM, including flexion, extansion, supination, pronation will be measured described by the American Academy of Orthopaedic Surgeons (AAOS) using a universal goniometer. The process will be repeated three times in each direction, with the the average value recorded.
Time frame: Baseline
The functional status of the patients will be evaluated by The Disabilities of the Arm, Shoulder and Hand (DASH).
Time frame: 1-month follow up
The functional status of the patients will be evaluated by The Disabilities of the Arm, Shoulder and Hand (DASH).
Time frame: Baseline
Pain intensity of the patients at rest, during activity, and at night will be assessed by Visual Analog Scale.
Time frame: After the six-week intervention
Pain intensity of the patients at rest, during activity, and at night will be assessed by Visual Analog Scale.
Time frame: 1-month follow up
Pain intensity of the patients at rest, during activity, and at night will be assessed by Visual Analog Scale.
Time frame: Baseline
Quality of life of the patients will be assessed by Short Form-12.
Time frame: After the six-week intervention
Quality of life of the patients will be assessed by Short Form-12.
Time frame: 1-month follow up
Quality of life of the patients will be assessed by Short Form-12.
Time frame: Baseline
Kinesiophobia of the patients will be assessed by Tampa Kinesiophobia Scale.
Time frame: After the six-week intervention
Kinesiophobia of the patients will be assessed by Tampa Kinesiophobia Scale.
Time frame: 1-month follow up
Kinesiophobia of the patients will be assessed by Tampa Kinesiophobia Scale.
Time frame: After the six-week intervention
Patient Satisfaction will be assessed with Global Rating of Change Scale.
Istanbul University
Other
The Efficacy of Proprioceptive Neuromuscular Facilitation Stretching and Static Stretching on Range of Motion, Pain and Function in Elbow Limitation
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