Comparison of the Efficacy of Manual Treatment according to Fascial Distortion Model Versus Joint Mobilization in Patients With Shoulder Impingement Syndrome

Comparison of the Efficacy of Manual Treatment According to Fascial Distortion Model Versus Joint Mobilization in Pain Reduction of Patients With Shoulder Impingement Syndrome Who Refer to Pirouzi Physiotherapy Clinic

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20200922048803N1

Enrollment

Registered

2021-04-20

Start date

2020-01-01

Completion date

Unknown

Last updated

2021-05-26

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

Conditions

Shoulder Impingement Syndrome. Impingement syndrome of shoulder

Interventions

Intervention 1: Intervention group: Three Sessions of Manual Treatment according to Fascial Distortion Model (Including Triggerband, Herniated Triggerpoint, Continuum, Folding, Cylinder And Tectonic)

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Pain By Arm Elevation With Intensity of =3 on VAS Positive Neer & Hawkins-Kennedy Tests

Exclusion criteria

Exclusion criteria: Stroke Rheumatoid Arthritis Full-thickness Rotator Cuff Tear Trauma Surgery of the Shoulder Freezing of the Shoulder Osteoporosis Malignancy

Design outcomes

Primary

Measure	Time frame
Pain Intensity. Timepoint: Before and after every treatment session and after a 2 week follow up. Method of measurement: Visual Analogue Scale.	—

Secondary

Measure	Time frame
Pain-free Abduction ROM. Timepoint: Before and after every treatment session and after a two week follow up. Method of measurement: Goniometry.;Function. Timepoint: Before the first treatment session, after the last session and after a two week follow up. Method of measurement: Persian Version of SPADI.;Patient Satisfaction With Treatment. Timepoint: After a two week follow up. Method of measurement: Likert Scale.	—

Measure

Time frame

Pain-free Abduction ROM. Timepoint: Before and after every treatment session and after a two week follow up. Method of measurement: Goniometry.;Function. Timepoint: Before the first treatment session, after the last session and after a two week follow up. Method of measurement: Persian Version of SPADI.;Patient Satisfaction With Treatment. Timepoint: After a two week follow up. Method of measurement: Likert Scale.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahmood Moradi

Tehran University of Medical Sciences

rehabilitation@tums.ac.ir+98 21 7753 3939

Outcome results

None listed

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