Skip to content

comparative effect of physiotherapy and corticosteroid injection on pain, disability and quality of life in patients with impingement syndrome

comparative effect of physiotherapy and corticosteroid injection on pain, disability and quality of life in patients with impingement syndrome

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180109038285N1
Enrollment
25
Registered
2018-12-04
Start date
2018-01-09
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

impingement syndrome. Bursitis of shoulder

Interventions

Intervention 1: Intervention group: Physiotherapy treatment group based on patient assessment and focus on the treatment of disorders. This treatment includes: correcting the body posture, strengtheni

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 68 Years

Inclusion criteria

Inclusion criteria: patients with impingement syndrome signs for more than 4 weeks pain level between 3 and 7 in VAS scale

Exclusion criteria

Exclusion criteria: full thickness rotator cuff tear neck pain adhesive capsulitis/ frozen shoulder history of shoulder girdle sublaxation or fracture in past 3 months

Design outcomes

Primary

MeasureTime frame
Shoulder pain and disability index,disability of arm shoulder hand. Timepoint: Pre and 4 weeks after randomization. Method of measurement: shoulder pain and disability index questionnaire, disability of arm, shoulder, hand questionnaire.

Secondary

MeasureTime frame
Pain intensity. Timepoint: pre and 4 weeks after randomization. Method of measurement: 10 cm ruler as measuring scale.;Quality of life. Timepoint: pre and 4 weeks after randomization. Method of measurement: western ontario rotator cuff index questionnaire.;Global rating of change. Timepoint: pre and 4 weeks after randomization. Method of measurement: question about effectiveness of treatment.;Disability of shoulder intensity. Timepoint: pre and 4 weeks after randomization. Method of measurement: SPADI and Quick-DASH questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDoctor Hossein Negahban sioki

Mashhad University of Medical Sciences

honegahban@yahoo.com+98 51 3884 6726

Outcome results

None listed

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