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OpenTrials
Completed

NCT Number: NCT05071469

Comparison of Two Different Treatment Methods

A number of previous studies investigated the effects of kinesiotaping (KT) in subacromial impingement syndrome (SIS).

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Key information

Conditions

Subacromial Impingement Syndrome Joint Diseases Muscle Weakness Muscular Diseases Musculoskeletal Diseases Musculoskeletal Injury Musculoskeletal Pain Nervous System Diseases Neurologic Manifestations Neuromuscular Manifestations Pain Pathologic Processes Pathological Conditions, Signs and Symptoms Shoulder Impingement Syndrome Shoulder Injuries Signs and Symptoms Weakness, Muscle Wounds and Injuries

Age range

35 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Muğla Sıtkı Koçman University

Muğla, 48000, Turkey (Türkiye)

About this study

Subacromial impingement syndrome (SIS) is characterized by shoulder pain that is exacerbated with especially arm elevation or overhead physical activities.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Impingement symptoms in clinical tests
  • Pain >1 month

Exclusion criteria

  • Any shoulder pathology.
  • Have chronic systemic diseases or infections.
  • History of any surgery shoulder complex.
  • steroid injections and therapeutic approaches

Treatment and study plan

Kinesiotaping

Other

KT was applied.

mulligan mobilization technique

Other

MMT was applied

Primary outcomes

  1. Change of pain severity

    Time frame: Baseline- after 2 weeks (after treatment)

    Via VAS.

  2. Change of Range of Motion

    Time frame: Baseline- after 2 weeks (after treatment)

    Via goniometer.

  3. Change of Functionality

    Time frame: Baseline- after 2 weeks (after treatment)

    Via SPADI.

Secondary outcomes

  1. Change of Sleep Quality

    Time frame: Baseline- after 2 weeks (after treatment)

    Via VAS.

  2. Change of Satisfaction of Life

    Time frame: Baseline- after 2 weeks (after treatment)

    Via SWLS.

  3. Change of Satisfaction of Treatment

    Time frame: Baseline- after 2 weeks (after treatment)

    Via VAs.

Sponsors and collaborators

Lead sponsor

Banu BAYAR

Other

Collaborators

  • Muğla Sıtkı Koçman University

Registry information

Official study title

Comparison of Short-term Effects of Two Different Treatment Methods in Patients With Subacromial Impingement Syndrome: a Randomized Controlled Single-blind Trial

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Oct 8, 2021
Registry last updated
Dec 21, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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