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Trial to Compare the Effectiveness of Group Versus Individual Therapy on Alternate Days in Patients With Subacromial Impingement Syndrome

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02833779
Enrollment
89
Registered
2016-07-14
Start date
2010-04-30
Completion date
Unknown
Last updated
2016-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mobility

Brief summary

Pathology of the rotator cuff and subacromial bursa is considered to be the principal cause of pain and symptoms arising from the shoulder. Physiotherapy specialists often disagree about which type of exercise is most appropriate. Manual Physiotherapy combined with guided exercise is a commonly applied clinical treatment, but no proof of its effectiveness has been shown. Clinical trials comparing results of treating subacromial syndrome of the shoulder with guided self-treatment and conventional physiotherapy yielded a slightly higher improvement, basically because patients suffered from chronic tendinitis and the treatment period lasted only two weeks. That is the reason why the investigators propose a long-term follow-up study and a more complete assessment of effectiveness of the exercise prescribed to improved this pathology. Objectives: * Assessment of effectiveness of two different types of treatment of subacromial syndrome of the shoulder. * Comparison of effectiveness of both treatments in order to select that one yielding better results as the one to be applied as a routine practice. Patients will be assigned one of the following treatments: * Group 1: patients will be taught exercises in groups of six people, on a daily basis for twelve sessions. * Group 2: patients will be taught the same exercise as Group 1, individually, and will receive manual therapy consisting of muscular and joint re-centering. A modified version of the Constant scale will be used to assess mobility and pain shoulder.

Interventions

OTHERIndividual exercises

Sponsors

Basque Health Service
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* History of shoulder pain defined as at least 2 positive results in subacromial impingement tests. * Self-perceived pain reported by the patient under clinical examination of the shoulder. * A minimum of 90º mobility in flexion.

Exclusion criteria

* Luxation, a history of surgery, or evidence the current shoulder pain or other symptoms under cervical examination or other shoulder bone disease, except for acromioclavicular joint arthrosis. * Patients were receiving other physiotherapy or rehabilitation treatments. * Patients had been treated for SIS (subacromial impingement syndrome) with injection of anti-inflammatory or analgesic drugs in the last month.

Design outcomes

Primary

MeasureTime frame
The assessment of pain with a visual analogue scale.Six Months
The mobility (joint range of motion) with a goniometer.Six Months

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026