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Conservative management of subacromial impingement syndrome in dialysis patients

The Comparision of kinesio taping & mobilisition on pain, rang of motion & shoulder disability in subacromial impingement syndrome in dialysis patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20091214002851N5
Enrollment
40
Registered
2020-10-18
Start date
2020-12-05
Completion date
Unknown
Last updated
2020-11-09

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

Conditions

Subacromial impingement syndrome in dialysis patients. Impingement syndrome of shoulder

Interventions

Intervention 1: Intervention group: mobilization and kinsiotape. Intervention 2: Control group: mobilization.

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 60 Years

Inclusion criteria

Inclusion criteria: positive of at least one subacromial syndrome tests (Neer, Hawkins, painful arc) dialysis more than 6 months shoulder pain more than 2 months anterior and anterior-lateral shoulder pain age between 40 to 60 years

Exclusion criteria

Exclusion criteria: Corticosteroid injection in the last 3 months neck radiculopathy pain history of trauma and shoulder fracture in the last 6 months history of shoulder and breast surgery positivity of TOS test pregnancy cancer kensiotape sensitivity physiotherapy in the last 3 months rheumatoid arthritis Non-steroidal anti-inflammatory drugs medication

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: Before the intervention, one month after the starting of the intervention and 10 days after the end of the intervention. Method of measurement: visual analog scale.

Secondary

MeasureTime frame
Active ROM of shoulder. Timepoint: Before the intervention, one month after the starting of the intervention. Method of measurement: goniometer.;Pain intensity and functional disability of shoulder. Timepoint: Before the intervention, one month after the starting of the intervention and 10 days after the end of the intervention. Method of measurement: DASH Questioner.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactmona ramezani

Babol University of Medical Sciences

ramzanimona@yahoo.com+98 11 3219 4641

Outcome results

None listed

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