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NCT05651048 Clinical Trial

The Role of BEMER and Kinesiotape in Increasing the Effectiveness of Physiotherapy and Rehabilitation Program After Videothoracoscopy Surgery

Pain, Post Operative Clinical Trial

Official title:
The Role of BEMER and Kinesiotape in Increasing the Effectiveness of Physiotherapy and

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT05651048
Other study ID # ICU-KARCI-3477
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date November 1, 2020
Est. completion date December 20, 2022

Study information
Verified date December 2022
Source Istanbul University - Cerrahpasa (IUC)
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The literature indicates that postoperative pulmonary complications are seen when pain is not treated effectively after videothoracoscopy surgery (VATS). After surgery, physiotherapy and rehabilitation approaches are applied to prevent complications. Bio-Electro-Magnetic-Energy-Regulation (BEMER) therapy uses low-frequency electromagnetic energy to regulate vasomotion in capillaries and increase microcirculation. BEMER therapy can be applied together with physiotherapy and rehabilitation. The aim of this study is to investigate the effectiveness of BEMER application, which is added to the physiotherapy and rehabilitation program applied after videothoracoscopy surgery.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 45
Est. completion date December 20, 2022
Est. primary completion date February 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Inclusion criteria for the study were to have undergone VATS lobectomy and to be aged between 18 and 75 years. Exclusion Criteria: - Presence of pacemaker, severe cardiac failure, severe arrhythmia - Those with cooperative disorders - Presence of neurological or orthopedic problems affecting the extremities - Those with severe psychiatric disorders - Failure to perform the operation according to the result of intraoperative tumor staging - Patients who go out of the standard Analgesia protocol - Patients who were taken back from the service to the intensive care unit

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Control Group
Physiotherapy and Rehabilitation Program After Videothoracoscopy Surgery
• BEMER Group
BEMER therapy and Physiotherapy and Rehabilitation Program After Videothoracoscopy Surgery
• Kinesiotape Group
Kinesiotape application and Physiotherapy and Rehabilitation Program After Videothoracoscopy Surgery

Locations
Country Name City State
Turkey Istanbul University - Cerrahpasa I?stanbul

Sponsors (1)
Lead Sponsor Collaborator
Istanbul University - Cerrahpasa (IUC)

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Change From Baseline in Pain Scores Change From Baseline in Pain Scores on the Visual Analog Scale at Postoperative 4th day Postoperative 4th day
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