Transcutaneous Pulse Radiofrequency Treatment for Subacromial Impingement Syndrome
NCT ID: NCT04289610
Last Updated: 2021-08-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
55 participants
INTERVENTIONAL
2020-03-03
2021-08-01
Brief Summary
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Detailed Description
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The study will be conducted between January 2020 and January 2021 at Gazi University Faculty of Medicine, Department of Physical Medicine and Rehabilitation. Fifty patients with subacromial impingement syndrome are planned to be recruited for the study.
The patients included in the study will be randomized into two groups with a computer program. In order to comply with the double-blind study protocol, the researcher performing the randomization of the patients will not participate in the treatment and evaluation processes. Demographic data of patients will be recorded at the beginning of the study. Therapeutic exercises and nonsteroidal anti-inflammatory drug therapy will be initiated to all patients. Detailed shoulder joint range of motion examination, visual analog scale, shoulder pain and disability index, quality of life scale (SF-36), shoulder ultrasound examination for acromio-humeral distance and supraspinatus tendon thickness measurements will be performed before and after treatment (Basal, 1st, 4th and 12th weeks). A pair of TCPRF electrodes will be applied to the painful shoulder at six standardized sites for 2 minutes each (approximately a total of 15 minutes). The device is not going to be activated in the control group. It will be activated in the study group. In the study group device will be set at 80 V, every pulse will continue for 10 milliseconds and 5 pulses per second. In the control group the device will be set at 0 V. TCPRF treatment is going to be applied for one session in both groups. During the three-month follow-up period, therapeutic exercises and as long as it is considered necessary nonsteroidal anti-inflammatory drugs will be continued in both groups.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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Control Group
In this group a pair of TCPRF electrodes will be applied to the painful shoulder at six standardized sites for 2 minutes each (approximately a total of 15 minutes). The device is not going to be activated in the control group. The device will be set at 0 V. TCPRF treatment is going to be applied for one session.
Transcutaneous pulse radiofrequency therapy
Transcutaneous pulse radiofrequency therapy (TCPRF) is a painless and outpatient physiotherapy modality
Study Group
A pair of TCPRF electrodes will be applied to the painful shoulder at six standardized sites for 2 minutes each (approximately a total of 15 minutes). It will be activated in the study group. In the study group device will be set at 80 V, every pulse will continue for 10 milliseconds and 5 pulses per second. TCPRF treatment is going to be applied for one session in both groups.
Transcutaneous pulse radiofrequency therapy
Transcutaneous pulse radiofrequency therapy (TCPRF) is a painless and outpatient physiotherapy modality
Interventions
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Transcutaneous pulse radiofrequency therapy
Transcutaneous pulse radiofrequency therapy (TCPRF) is a painless and outpatient physiotherapy modality
Eligibility Criteria
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Inclusion Criteria
* Having (chronic) shoulder pain for more than 3 months
* No treatment for shoulder pain (physical therapy, joint area injection, radiofrequency treatment) in the past 3 months
Exclusion Criteria
* Malignancy, acute infections Adhesive capsulitis
* Bicipital tendinitis
* Supraspinatus tendon full-thickness rupture
* Those who have undergone surgery for shoulders and neck
* Pace maker
* Pregnant women Those with cervical radiculopathy
* Those who do not agree to participate in the study
18 Years
65 Years
ALL
No
Sponsors
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Gazi University
OTHER
Responsible Party
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Ayça Utkan Karasu
medical doctor, principal investigator
Locations
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Gazi University Medical School, Physical Medicine and Rehabilitation Department
Ankara, , Turkey (Türkiye)
Countries
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References
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Taverner M, Loughnan T. Transcutaneous pulsed radiofrequency treatment for patients with shoulder pain booked for surgery: a double-blind, randomized controlled trial. Pain Pract. 2014 Feb;14(2):101-8. doi: 10.1111/papr.12059. Epub 2013 Apr 8.
Kul A, Ugur M. Comparison of the Efficacy of Conventional Physical Therapy Modalities and Kinesio Taping Treatments in Shoulder Impingement Syndrome. Eurasian J Med. 2019 Jun;51(2):139-144. doi: 10.5152/eurasianjmed.2018.17421. Epub 2018 Nov 30.
Taverner MG, Ward TL, Loughnan TE. Transcutaneous pulsed radiofrequency treatment in patients with painful knee awaiting total knee joint replacement. Clin J Pain. 2010 Jun;26(5):429-32. doi: 10.1097/AJP.0b013e3181d92a87.
McCreesh KM, Anjum S, Crotty JM, Lewis JS. Ultrasound measures of supraspinatus tendon thickness and acromiohumeral distance in rotator cuff tendinopathy are reliable. J Clin Ultrasound. 2016 Mar-Apr;44(3):159-66. doi: 10.1002/jcu.22318. Epub 2015 Dec 15.
Other Identifiers
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Gazi University PMR
Identifier Type: -
Identifier Source: org_study_id
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