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Efficiency of Hypervolt Device Application in the Treatment of Shoulder Impingement Syndrome

Not Applicable
Completed
Conditions
Shoulder Impingement
Interventions
Other: Physiotherapy
Other: Hypervolt Device
Registration Number
NCT06006351
Lead Sponsor
Uskudar University
Brief Summary

The aim of this study is to compare the effects of exercise and Hypervolt Device on pain, muscle strength and normal joint movement in the treatment of shoulder impingement syndrome.

Detailed Description

The study was planned as a randomized controlled trial. The study sample will be divided into two groups by simple randomization method. Only exercise will be applied to 30 individuals diagnosed with shoulder impingement in the first group of the study. In the second group, 30 individuals with shoulder impingement diagnosis will be given a Hypervolt Device in addition to the exercise. Disabilities of the Arm, Shoulder and Hand Questionnaire, Visual Analog Scale and Lawton Daily Living Activities Questionnaire will be applied to the participants before and after the treatment. The obtained data will be analyzed statistically.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Being between the ages of 18-50.
  • Having a Visual Analogue Scale (VAS) value of 5 or higher.
  • Having a history of shoulder pain for at least 1 month.
  • Volunteer to participate in research.
  • Having been diagnosed with Shoulder Impingement.
Exclusion Criteria
  • Having cognitive, mental or psychological problems.
  • Having a condition that prevents him from exercising.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
MassageHypervolt DeviceIn addition to the classical physiotherapy protocol, a Hypervolt Device will be applied.
controlPhysiotherapyclassical physiotherapy protocol will be applied.
MassagePhysiotherapyIn addition to the classical physiotherapy protocol, a Hypervolt Device will be applied.
Primary Outcome Measures
NameTimeMethod
Disabilities of the Arm, Shoulder and Hand Questionnaire12 weeks

It was developed to evaluate functional status and symptoms by focusing on physical function in upper extremity injuries. According to the results of the survey; a result from 0-100 is obtained from each part; 0-no apology 100-maximum apology.

Lawton Activities of Daily Living Scale12 weeks

It is a questionnaire consisting of eight questions, including information about using the telephone, preparing food, shopping, doing daily household chores, washing clothes, getting on a transportation vehicle, using medicines and managing money. If the individual does the activities independently, three points, two points if he does it with help, and one point if he cannot do it at all. In Lawton Activities of Daily Living Scale; 0-8 points are classified as "dependent", 9-16 points as "semi-dependent", 17-24 points as "independent".

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Uskudar university

🇹🇷

Istanbul, Turkey

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