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

Not Applicable
Active, not recruiting
Conditions
Pain, Post Operative
Interventions
Other: Kinesiotape Group
Other: BEMER Group
Other: Control Group
Registration Number
NCT05651048
Lead Sponsor
Istanbul University - Cerrahpasa (IUC)
Brief 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
45
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

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Kinesiotape GroupKinesiotape GroupKinesiotape application with routine treatment protocol
BEMER GroupBEMER GroupBEMER application with routine treatment protocol
Control GroupControl Grouproutine treatment protocol
Primary Outcome Measures
NameTimeMethod
Change From Baseline in Pain ScoresPostoperative 4th day

Change From Baseline in Pain Scores on the Visual Analog Scale at Postoperative 4th day

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Istanbul University - Cerrahpasa

🇹🇷

İ̇stanbul, Turkey

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