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Investigation of effect of Physiotherapy on surgery candidate patients with full thickness tear of Supraspinatpus tendon

Investigation of effect of Physiotherapy on some clinical parameters of surgery candidate patients with full thickness tear of Supraspinatpus tendon

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014081018754N1
Enrollment
15
Registered
2014-11-23
Start date
2014-11-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Supraspinatus Tear. Rotator cuff syndrome

Interventions

A physiotherapy protocol which included 3 basic phase will execute for all surgery candidate patients who will participate in the present study. Each phase will last for 3 to 4 weeks depend on improve
Rehabilitation

Sponsors

Vice chancellor for research, Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Non-traumatic full tear of Supraspinatous tendon according to physician refer; positive sign of impingement; presentation of sign and symptoms for more than 6 months. These subjects will not include in the study: Any injury of shoulder girdle complex (other than inclusion criteria); Degenerative Joint Diseases or Arthritis of shoulder complex; tendon tear of other muscles (except Supraspinatous tendon); recurrent dislocation of shoulder; fracture and stiffness of shoulder capsule. Exclusion criteria: If a patient dose not complete the Physiotherapy program; missing the sessions for more than two. *The patient will stop his/she program any time he/she wants.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Shoulder Pain. Timepoint: Before the intervention, 20th session and at the end of intervention (30th session). Method of measurement: VAS.;Shoulder Function. Timepoint: Before the intervention, 20th session and at the end of intervention (30th session). Method of measurement: QuickDASH questionnaire.;Passive and active range of motion of shoulder. Timepoint: Before the intervention, 20th session and at the end of intervention (30th session). Method of measurement: Goniometer.;Strength of shoulder muscles. Timepoint: Before the intervention, 20th session and at the end of intervention (30th session). Method of measurement: Dynamometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactJavad Sarrafzadeh

Iran University of Medical Sciences

sarrafzadeh.j@iums.ac.ir+98 21 2222 8051

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026