Lateral Epicondylitis Clinical Trial
Official title:
Influence of Proximal Motor Control in Treating Lateral Epicondylitis
This study will be conducted to investigate the effect of scapular muscles (lower trapezius, middle trapezius and serratus anterior) strengthening on pain, pain free hand grip strength and functional outcome added to conventional physical therapy in patients with chronic Lateral Epicondylitis.
Status | Not yet recruiting |
Enrollment | 52 |
Est. completion date | November 1, 2022 |
Est. primary completion date | October 15, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 30 Years to 50 Years |
Eligibility | Inclusion Criteria: 1. Symptoms of lateral epicondylitis from at least the past 3 months. 2. Pain in at least two of the following four tests; Tomsen test, Maudsley test, Mill's test and handgrip dynamometer test. 3. Their ages range from 30-50 years old. Exclusion Criteria: Subjects will be excluded from the study if they have: 1. Peripheral neuropathy. 2. Lesions of upper limb nerves. 3. History of surgery in the affected elbow 6 months ago. 4. Cervical radiculopathy. |
Country | Name | City | State |
---|---|---|---|
Egypt | Outpatient clinic, Faculty of Physical Therapy, Cairo university | Dokki |
Lead Sponsor | Collaborator |
---|---|
Cairo University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Assessment of change in pain intensity | Using Visual analouge scale (VAS), a continuous 10 cm line ranges from no pain to very severe pain which is valid and reliable tool. The patient marks on the line the point that they feel represents their pain intensity. | at baseline and after 6 weeks of intervention | |
Primary | Assessment of change in hand grip strength | Patient stands with the elbow in complete extension and the shoulder and radioulnar joints in neutral rotation. Ask the patient to slowly squeeze the dynamometer and to stop the instant discomfort is first felt. It will be performed three repetitions separated by a 20-second rest interval. Average of three trials will be recorded. The measurement is valid and reliable. | at baseline and after 6 weeks of intervention | |
Primary | Assessment of change in function | Using PRTEEQ. It is a 15-item self-reported questionnaire to measure perceived pain and disability in people with LE. It has three subscales: pain, usual activities and specific activities. Each of the items of the Patient rated tennis elbow evaluation questionnaire (PRTEEQ) is scored on a 0-10 scale, where 0 is 'no pain' or 'no difficulty' and10 is 'worst ever' or 'unable to do. Ask the patients to rate the pain and difficulty that they have experienced in the last week by marking the suitable response that reflects their current state. The total score ranges from 0 to 100, where high scores indicate greater pain and disability. | at baseline and after 6 weeks of intervention |
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