Skip to content

Effectiveness of a protected activation exercise program in patients with arthroscopic rotator cuff surgery

Effectiveness of a supervised early exercise program in patients with arthroscopic rotator cuff repair: Randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-5m42mh
Enrollment
Unknown
Registered
2018-12-18
Start date
2019-09-02
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Shoulder rotator cuff tendon tear

Interventions

59 patients with total rupture of the supraspinatus muscle subjected to an arthroscopic repair with anchorage and / or simple suture, on the second day, after surgery, we began with a protected activa
Periodicity 2 to 3 times per week
Treatment duration 6 weeks. Control Group: 59 subjects, Begin the sixth week after surgery and perform a conventional treatment program of 12 sessions consisting of a series of glenohumeral and scapul
Treatment duration 6 weeks.
Other
E02.779.474

Sponsors

CDT Hospital San Borja de Arriaran
Lead Sponsor
Universidad de las Americas
Collaborator

Eligibility

Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Subjects of both genders; whose age range is between 18 and 55 years with medical diagnosis of total rupture of the supraspinatus muscle, based on clinical and imaging criteria (ECOTOMOGRAPHY and MRI); submitted to arthroscopic repair with simple suture by the team of Traumatologists of the HCSB Arriarán; accept and sign the informed consent.

Exclusion criteria

Exclusion criteria: subjects with massive rotator cuff tear (2 or more tendons and / or injury greater than 5 cm) and with presence of associated lesions Example; Glenohumeral Instability; Adhesive Capsulitis; Cervical Hernia etc.

Design outcomes

Primary

MeasureTime frame
Function The function will be evaluated using the Constant-Murley questionnaire, which is one of the most used and recommended instruments to evaluate the function of the shoulder.

Secondary

MeasureTime frame
functionality To assess the functionality of the EESS, the DASH questionnaire, originally created by Hudak et al, was used to assess disability and symptoms in people with musculoskeletal disorders of the EESS. To monitor adherence to treatment, patients will be contacted by telephone at the 4th and 8th week of treatment.;Pain The visual analogue scale (VAS) will be used to assess the intensity and movement of pain at rest. To monitor adherence to treatment, patients will be contacted by telephone at the 4th and 8th week of treatment.;The range of motion of anterior flexion, abduction and external glenohumeral rotation, for which it will occupy the goniometry

Countries

Chile

Contacts

Public ContactFelipe Araya

Universidad de las Americas

fandres.kine@gmail.com+5697122483

Outcome results

None listed

Source: REBEC (via WHO ICTRP)