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

Comparison of the Effects of Exercise and Hypervolt Device Application on Pain, Muscle Strength and Normal Joint Movement in the Treatment of Shoulder Impingement Syndrome

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06006351
Enrollment
30
Registered
2023-08-23
Start date
2023-09-01
Completion date
2023-12-01
Last updated
2023-12-22

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

Conditions

Shoulder Impingement

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.

Interventions

OTHERPhysiotherapy

manual therapy stretching exercises strengthening exercises electrotherapy applications

OTHERHypervolt Device

The painful area will be applied with a massage tool, and the frequency and mode of the tool will be adjusted in a way that does not disturb the patient.

Sponsors

Uskudar University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Intervention model description

Exercise therapy and Applying a Hypervolt massager

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Disabilities of the Arm, Shoulder and Hand Questionnaire12 weeksIt 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 weeksIt 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.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026