Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
42 participants
INTERVENTIONAL
2013-01-31
2014-01-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Inclusion of Mobilisation With Movement to an Exercise Programme in Rotator Cuff Related Pain
NCT04175184
Effects of Diaphragm Muscle Therapy on Pain and Shoulder Movement in Subjects With Rotator Cuff Injuries
NCT03293329
Mobilization and Mobilization With Movement Effect on Sub Acromial Space in Impingement Syndrome.
NCT04579003
Therapeutic Progressive Exercise on Shoulder Impingement Syndrome
NCT04690049
Manual Therapy in Chronic Shoulder Pain Treatment
NCT03416556
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Real mobilization-with-movement (MWM)
For the MWM group, an accessory posterior-lateral gliding movement in the humeral head combined with a movement of active shoulder flexion will be applied. One hand will be placed over the scapula posteriorly while the thenar eminence of the other hand will be placed over the anterior aspect of the head of the humerus
Real mobilization-with-movement (MWM)
Sham mobilization-with-movement (MWM)
The sham condition will replicate the treatment condition except for the hand positioning. The therapist locates one hand over the belly of the pectoralis major muscle and the other over scapula without applying any pressure. The patient will be asked to move the arm in a similar manner as in the MWM group
Sham mobilization-with-movement (MWM)
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Real mobilization-with-movement (MWM)
Sham mobilization-with-movement (MWM)
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* pain localized at the proximal anterolateral shoulder region
* medical diagnosis of shoulder impingement syndrome
* at least 2 positive impingement tests including Neer, Hawking, or Jobe test
Exclusion Criteria
* pregnancy
* a history of traumatic onset of shoulder pain
* other histories of shoulder injury
* ligamentous laxity based on a positive Sulcus test and apprehension test
* numbness or tingling in the upper extremity
* previous shoulder or cervical spine surgery
* corticosteroid injection on the shoulder within 1 year of the study
* physical therapy 6 months prior to the study
18 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Salamanca
OTHER
César Fernández-de-las-Peñas
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
César Fernández-de-las-Peñas
Proffesor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Francisco Alburquerque Sendín, PT, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Salamanca
César Fernández de las Peñas, PT, PhD
Role: STUDY_CHAIR
Universidad Rey Juan Carlos
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Francisco Alburquerque Sendín
Salamanca, Salamanca, Spain
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
USAL201000048540
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.