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The effect of kinesiotype and corrective movements on pain and shoulder function in impingement syndrome of shoulder

Comparative study of the effect of kinesiotype and corrective movements on pain and shoulder function in impingement syndrome of shoulder

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200825048515N3
Enrollment
50
Registered
2020-09-21
Start date
2020-10-22
Completion date
Unknown
Last updated
2020-10-06

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

Conditions

Impingement syndrome of shoulder. Impingement syndrome of shoulder

Interventions

Intervention 1: Intervention group: For all patients, meloxicam 15 mg tablets daily, as well as baclofen tablets, half a tablet on the first night and on the following nights, one tablet every night w

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age over 18 years Diagnosis of impingement syndrome of shoulder by a physical therapist Satisfaction to participate in the study

Exclusion criteria

Exclusion criteria: 1. History of dislocation and traumatic injury and history of surgery on the shoulder joint Deformity of the scapula and hunched back with the diagnosis of a physician specializing in physical medicine Rotator cuff muscle rupture Shoulder joint instability Neurological problems of the neck, such as neck radiculopathy Rheumatic diseases and destructive changes in the joints History of shoulder injection or shoulder or neck physiotherapy in the last six months by reviewing the patient's medical record History of neurological diseases such as stroke, multiple sclerosis The presence of any skin disease around the shoulder and scapula

Design outcomes

Primary

MeasureTime frame
Shoulder pain. Timepoint: Before and three weeks after the intervention. Method of measurement: Visual analog scale(VAS).;Shoulder function. Timepoint: Before and three weeks after the intervention. Method of measurement: By criteria Disabilities of the Arm, Shoulder and Hand (DASH).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParisa Taheri

Esfahan University of Medical Sciences

Prs_taheri@yahoo.com+98 31 3668 5555

Outcome results

None listed

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