Status:
UNKNOWN
The Effect of Reiki and Acupressure on Pain, Anxiety and Vital Signs
Lead Sponsor:
Mersin University
Conditions:
Coronary Artery Disease
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
This research aims to determine the effects of reiki and acupressure applied after percutaneous coronary intervention on pain, anxiety and vital signs during femoral catheter extraction.
Detailed Description
In this study, 84 patients with percutaneous coronary intervention were assigned to the reiki, acupressure and control groups by block randomization method.In the acupressure group (n=28) the heart me...
Eligibility Criteria
Inclusion
- 18 years and over,
- Percutaneous coronary intervention (PCI) for the first time,
- Previously planned PCI (elective patients),
- No additional procedure to percutaneous coronary intervention,
- Awake and conscious during percutaneous coronary intervention (not taking sedatives)
- A single sandbag is placed on the intervention area,
- Able to lie flat on his back (without respiratory distress),
- Hemodynamically stable (absence of chest pain and arrhythmia),
- No analgesic drug administered at least four hours before,
- No complications such as hematoma or bleeding in the operation area,
- No deformity or lesion in the areas where acupressure will be applied,
- No previous experience of acupressure and reiki application,
- Not diagnosed with anxiety disorder and not receiving medical treatment,
- Literate,
- Have sufficient communication skills and
- Those who signed the Informed Consent Form to participate
Exclusion
- Emergency patients whose PCI was not planned beforehand,
- Bleeding, hematoma, etc. at the femoral intervention site during and after the procedure. developing complications,
- Any deformity, wound or lesion in the areas where acupressure will be applied,
- Coronary angiography only,
- Thrombocyte level less than 100,000 mg/dl,
- Those who did not sign the Informed Consent Form to participate in the study
Key Trial Info
Start Date :
May 15 2022
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
November 15 2022
Estimated Enrollment :
84 Patients enrolled
Trial Details
Trial ID
NCT05381246
Start Date
May 15 2022
End Date
November 15 2022
Last Update
May 19 2022
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