Manual Therapy in Chronic Shoulder Pain Treatment
- Conditions
- Shoulder Pain
- Interventions
- Procedure: The manual contact conditionProcedure: Mobilization to the glenohumeral jointOther: No-contact condition
- Registration Number
- NCT03416556
- Lead Sponsor
- University of Alcala
- Brief Summary
Background: Passive oscillatory mobilizations are often employed by physiotherapists to reduce shoulder pain and increase function. However, there is little data about the neurophysiological effects of these mobilizations.
Objectives: To investigate the initial effects of an anteroposterior (AP) shoulder joint mobilization on measures of pain and function in overhead athletes with chronic shoulder pain.
- Detailed Description
Design: Double-blind, controlled, within-subjects repeated-measures design Method: Thirty-one overhead athletes with chronic shoulder pain participated. The effects of a 9-min, AP mobilization of the glenohumeral joint were compared with manual contact and no-contact interventions. Pressure pain threshold (PPT), range of movement (ROM), muscle strength, self-reported pain, and disability were measured immediately before and after each intervention.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 31
- History of chronic shoulder pain lasting ≥3 months.
- Play overhead sport regularly.
- Had a non-musculoskeletal origin of shoulder pain.
- Previous surgery to the shoulder complex.
- Frozen shoulder.
- Any co-existing inflammatory, infectious or neurological condition.
- The patient from physiotherapy treatment.
- Any evidence of pain referred from the cervical spine to the shoulder
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description The manual contact condition The manual contact condition In this condition the therapist positioned the patient in a mid-range position of glenohumeral abduction and internal rotation and applied the hands to the same contact point as in the treatment condition. Mobilization to the glenohumeral joint Mobilization to the glenohumeral joint This condition consisted on the application of a passive rhythmic AP mobilization to the glenohumeral joint of the affected shoulder The manual contact condition No-contact condition In this condition the therapist positioned the patient in a mid-range position of glenohumeral abduction and internal rotation and applied the hands to the same contact point as in the treatment condition.
- Primary Outcome Measures
Name Time Method Self-reported shoulder pain Change from Baseline at 5 minutes after intervention Participants were asked to indicate the intensity of their current shoulder pain using a numeric rating pain scale (NRPS). In this scale, 0 is not pain and 10 is the worse pain possible
- Secondary Outcome Measures
Name Time Method Shoulder disability Change from Baseline at 24 hours after treatment The DASH is comprised of 30 items (disability/symptom section) and two optional sections related to the impact of pathology on work and sports. Each item is scored from 1 to 5 with increasing values representing more severity of symptoms. The total score for the disability/symptoms section ranges from 30 to 150, but it is then transformed to a scale from 0 (better score possible) to 100 (worse score possible).
Shoulder range of movement (ROM) Change from Baseline at and 5 minutes after treatment Active elevation in the scapular plane and passive glenohumeral internal and external rotation were measured using a Standard BASELINE ® 12-inch plastic goniometer following previous guidelines. The 0 degrees of movement is worse and 180 degrees is the better
Shoulder muscles strength Change from Baseline at 5 minutes after treatment Isometric strength of the shoulder internal and external rotator musculature was measured using a portable hand-held dynamometer (Nicholas Manual Muscle Tester, Lafayette Instruments, USA). Normal external rotation strength is 20 Newtons and 27 newton in internal rotation strength
Pressure pain threshold (PPT) Change from Baseline at 5 minutes after treatment The PPT was measured using an analogue Fisher algometer (Force Dial model FDK, Wagner Instruments) with a surface area at the round tip of 1cm2. The algometer probe tip was applied perpendicular to the skin at a rate of 1kg/cm2/s until the first onset of pain. The PPT value is specific in each subject.The minimal clinically important difference is 2Kg/cm
Trial Locations
- Locations (1)
Clinical University
🇪🇸Alcala de Henares, Madrid, Spain