Manual Therapy, Exercise and US Vs. Manual Therapy, Exercise and US for Medial Epicondylalgia
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Electric Dry Needling, Manual Therapy, Exercise and Ultrasound, Manual Therapy, Exercise and Ultrasound.
- Who it may be relevant to
- Registry conditions: Epicondylalgia. Basic parameters: 18 years — 60 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Manual Therapy, Exercise and Ultrasound Vs. Manual Therapy, Exercise, Ultrasound and Electric Dry Needling for Patients With Medial Epicondylalgia
Overview
The purpose of this research is to compare two different approaches for treating patients with medial epicondylalgia: manual therapy, exercise and ultrasound and manual therapy, exercise, ultrasound and electric dry needling. Physical therapists commonly use all of these techniques to treat medial epicondylalgia. This study is attempting to find out if one treatment strategy is more effective than the other.
Detailed description
Patients with medial epicondylalgia will be randomized to receive 8 treatments (2 treatments per week) over 4 weeks (8 treatments max) of either: 1. manual therapy, exercise and ultrasound or 2. manual therapy, exercise, ultrasound and electric dry needling
Interventions
- Other Electric Dry Needling, Manual Therapy, Exercise and Ultrasound
Electric Dry Needling, Manual Therapy, Exercise and Ultrasound - Other Manual Therapy, Exercise and Ultrasound
Electric Dry Needling, Manual Therapy, Exercise and Ultrasound vs. Manual Therapy, Exercise and Ultrasound
Primary outcome measures
- Change in elbow pain intensity (NPRS) [Time frame: Baseline, 1-week, 4-weeks, 3-months]
Secondary outcome measures (3)
- Disabilities of the Arm, Shoulder and Hand [Time frame: Baseline, 1-week, 4-weeks, 3-months]
- Change in Global rating of change score [Time frame: 4-weeks, 3-months]
- Change in Medication Intake (Frequency of Medication Intake in last week) [Time frame: Baseline, 3-months]
Eligibility criteria
Inclusion criteria
- Adult between18 and 60 years old that is able to speak English.
- Report of at least 6 weeks of elbow (i.e. medial epicondyle) and ventral forearm pain, consistent with medial epicondylalgia.
- Patient has not had physical therapy, massage therapy, chiropractic treatment or injections for elbow pain in the last 6 months.
- Diagnosis of medial epicondylalgia, defined as the following:(Walz, 2010; Shin, 2019)
- Tenderness is elicited by palpation of the insertion of the flexor-pronator mass (5-10 mm distal and anterior to the middle aspect of the medial epicondyle)
- Pain is exacerbated by resisted wrist flexion and forearm pronation at an angle of 90°
Exclusion criteria
- Report of red flags to manual physical therapy to include: severe hypertension, infection, uncontrolled diabetes, peripheral neuropathy, heart disease, stroke, chronic ischemia, edema, severe varicosities, tumor, metabolic disease, prolonged steroid use, fracture, RA, osteoporosis, severe vascular disease, malignancy, etc.
- Report of Previous surgery of the elbow, history of elbow dislocation, elbow fracture and/or tendon rupture.
- History of or presentation consistent with osteochondritis dissecans, osteoarthrosis, MCL injury (i.e. Pain with valgus stress or positive "milking test" - pulling on the thumb with the elbow in flexion and the forearm in supination), flexor-pronator strain, and ulnar neuropathy (i.e. Positive Tinel sign - distal pain and tingling during direct compression of the nerve at the elbow).
- Report of systemic neurological disorders and/or neurological deficits to include the following: a. Nerve root compression (muscle weakness involving a major muscle group of the upper extremity, diminished upper extremity deep tendon reflex, or diminished or absent sensation to pinprick in any upper extremity dermatome) b. Cervical or thoracic spinal stenosis (exhibited by bilateral upper extremity symptoms) c. Central nervous system involvement (hyperreflexia, sensory disturbances in the hand, intrinsic muscle wasting of the hands, unsteadiness during walking, nystagmus, loss of visual acuity, impaired sensation of the face, altered taste, the presence of pathological reflexes) d. History of whiplash or T-spine injury injury within the previous 6 weeks 5. History of surgery to the head/neck/T-spine or affected upper extremity.
6\. Psychiatric disorders or cognitively impaired 7. Pregnancy
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Double blind
- Primary purpose
- Treatment
Study locations
United States · 1 center
- Mallers and Swoverland Orthopedic PT — Fort Wayne
Identifiers
NCT: NCT04609735 · AAMT50