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
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COMPLETED
NA
31 participants
INTERVENTIONAL
2018-02-15
2018-03-15
Brief Summary
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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.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
DOUBLE
* Outcomes assessor did´t know the treatment applied to the participants
Study Groups
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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
Mobilization to the glenohumeral joint
The treatment condition consisted on the application of a passive rhythmic AP mobilization to the glenohumeral joint of the affected shoulder. In particular, a Grade III AP glide to the humeral head with the arm positioned in 90º of glenohumeral abduction and full internal rotation was used. The posterior gliding force to the humeral head was applied maintaining the glide at right angles to the plane of movement and at a frequency of 2 Hz which was controlled by means of a metronome. The arm was returned to its original position between each set.
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.
The manual contact condition
During the manual contact 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. However, a simulated posterior glide was performed but with minimal pressure actually applied. The number of repetitions and sets were as per the treatment condition.
No-contact condition
During the no-contact condition, the subject remained in the initial starting position thorough the entire session but there was no manual contact between the therapist and the participant. The total treatment time was the same as per the other conditions.
No-contact condition
There was no manual contact between the therapist and the participant
No interventions assigned to this group
Interventions
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Mobilization to the glenohumeral joint
The treatment condition consisted on the application of a passive rhythmic AP mobilization to the glenohumeral joint of the affected shoulder. In particular, a Grade III AP glide to the humeral head with the arm positioned in 90º of glenohumeral abduction and full internal rotation was used. The posterior gliding force to the humeral head was applied maintaining the glide at right angles to the plane of movement and at a frequency of 2 Hz which was controlled by means of a metronome. The arm was returned to its original position between each set.
The manual contact condition
During the manual contact 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. However, a simulated posterior glide was performed but with minimal pressure actually applied. The number of repetitions and sets were as per the treatment condition.
No-contact condition
During the no-contact condition, the subject remained in the initial starting position thorough the entire session but there was no manual contact between the therapist and the participant. The total treatment time was the same as per the other conditions.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Play overhead sport regularly.
Exclusion Criteria
* 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
18 Years
60 Years
ALL
No
Sponsors
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University of Alcala
OTHER
Responsible Party
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Prof. Dr. Daniel Pecos Martín
Professor
Principal Investigators
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Daniel Pecos-Martin, Dr
Role: PRINCIPAL_INVESTIGATOR
Alcala University
Locations
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Clinical University
Alcalá de Henares, Madrid, Spain
Countries
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Provided Documents
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Document Type: Study Protocol
Other Identifiers
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H1496053548524
Identifier Type: -
Identifier Source: org_study_id
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