Application of an Exercise Program Versus Exercise Plus Manual Therapy in the Treatment of Adhesive Capsulitis.
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Capsulitis of Shoulder
- Sponsor
- University of Alcala
- Enrollment
- 108
- Locations
- 1
- Primary Endpoint
- evaluation of the improvement of shoulder mobility in patients with adhesive capsulitis by performing by an exercise program, mobilization or boths techniques.
- Status
- Not yet recruiting
- Last Updated
- last year
Overview
Brief Summary
The main objective is to evaluate whether a treatment program combining manual therapy (joint mobilization) and exercise is more effective in the treatment of adhesive capsulitis than an exercise program applied in isolation.
The researchers will compare both groups (experimental group and control group) using the different techniques.
During the sessions, mobility will be evaluated with a goniometer and data will be recorded to monitor progress, maintaining a confidential record of the data.
Investigators
Cecilia Sánchez Pérez
principal investigator of the study Application of an exercise program versus exercise plus manual therapy in the treatment of adhesive capsulitis.
University of Alcala
Eligibility Criteria
Inclusion Criteria
- •men and women from 40 to 60 years old, whether or not they carry out physical activity
- •intervention through therapeutic exercise and/or joint mobility.
Exclusion Criteria
- •older people
- •people with previous shoulder pathology
- •people with cognitive impairment who cannot complete questionnaires
- •treatment that does not include exercise or joint mobility
- •treatment with machines.
Outcomes
Primary Outcomes
evaluation of the improvement of shoulder mobility in patients with adhesive capsulitis by performing by an exercise program, mobilization or boths techniques.
Time Frame: 3-4 months
study and measure if there is improvement in adhesive capsulitis of the shoulder with the proposed exercise programs versus exercise plus manual therapy in 108 subjects, 54 subjects in each group and a descriptive analysis of the data will be carried out, examining the initial homogeneity between the groups. in terms of the variables age, sex, pain, range of motion and functionality. The Shoulder Pain and Disability Index (SPADI) questionnaire and the visual analogue scale (VAS) will be used to assess pain.