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Effect of Reiki Applied After Coronary Angiography on Pain and Comfort Level

Not Applicable
Recruiting
Conditions
Coronary Angiography
Registration Number
NCT07193784
Lead Sponsor
Mersin University
Brief Summary

Coronary angiography is an invasive imaging technique that directly visualizes the anatomical structure of the coronary arteries and is considered the gold standard for diagnosing significant coronary artery disease. In the post-coronary angiography period, alleviating pain and enhancing patient comfort are important goals of clinical care. Reiki is an energy-based complementary therapy aimed at supporting the body's natural healing processes and promoting relaxation. Among non-pharmacological interventions, Reiki-a practice rooted in Traditional Chinese Medicine and meaning universal life energy-is a safe, cost-effective, and easily applicable method. Studies have shown that Reiki is effective in reducing pain, anxiety, fear, and stress, as well as in improving comfort and holistic well-being. This study was designed to examine the effects of Reiki therapy administered after coronary angiography on patients' levels of pain and comfort.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
90
Inclusion Criteria
  • Adults aged 18-80 years.
  • Undergoing coronary angiography for the first time.
  • No additional interventions (e.g., stent placement) performed during angiography.
  • Coronary angiography performed via femoral artery.
  • Elective (non-emergency) coronary angiography.
  • No prior experience with Reiki, Therapeutic Touch, or other energy therapies.
  • Able to understand and speak Turkish.
  • Open to communication and able to participate in face-to-face interviews.
Exclusion Criteria
  • Development of acute complications during or after coronary angiography (e.g., myocardial infarction, severe arrhythmia, embolism, bleeding at the intervention site, hematoma).
  • Any diagnosed psychiatric disorder.
  • History of chronic pain or regular use of analgesics.
  • Previous experience with Reiki or similar complementary therapies.
  • Requirement for sedative or opioid analgesic use during the study period.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Pain levelBaseline (before intervention), 30 minutes after intervention, 2 hours after intervention, and prior to first mobilization (within 24 hours).

Pain intensity measured using Visual Analog Scale (VAS, 0-10) via face-to-face interviews at the specified time points.

Secondary Outcome Measures
NameTimeMethod
Comfort levelBaseline (before intervention), 30 minutes after intervention, 2 hours after intervention, and prior to first mobilization (within 24 hours).

Comfort level was assessed using the "General Comfort Scale Short Form" through face-to-face interviews at the same locations.

Trial Locations

Locations (1)

Mersin University Hospital

Mersin, Turkey (Türkiye)

Mersin University Hospital
Mersin, Turkey (Türkiye)
Abdullah Avcı, PhD
Contact
+903242410000
abdullahavci@mersin.edu.tr

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