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NCT07175558Completed

Effects of Reiki Applied to Patients Undergoing Colorectal Cancer Surgery on Postoperative Pain, Anxiety, Physiological Parameters and Recovery

Source: ClinicalTrials.gov · Last updated 16 Sept 2025

Brief summary (registry, in English)

Reiki touch therapy has been used for many years, especially on pain, anxiety and physiological parameters, and studies have been found to show that it is effective. In a systematic review conducted with Sectio patients, it was determined that reiki reduces pain. In a study conducted by Zare et al. with patients undergoing coronary bypass surgery, it was reported that reiki regulates the respiratory rate. It was determined that reiki applied to the incision area in patients undergoing abdominal surgery reduces pain. In a different study, it was emphasized that reiki applied to 90 women who gave birth by cesarean section in the experimental group on the 1st and 2nd days after surgery decreased pain and anxiety levels, analgesic requirement and respiratory rate after surgery compared to the control group, while there was no change in blood pressure and pulse. In a meta-analysis study including four studies consisting of 104 patients in the Reiki group and 108 patients in the control group, a statistically significant decrease in the pain score of the Reiki group was found. In a study conducted by Bremner and colleagues, it was determined that stress, anxiety and depression decreased in the Reiki group. In a study measuring the effect of Reiki use on pain, stress and anxiety levels in patients undergoing total knee replacement surgery, significant decreases were found in pain, blood pressure, respiratory rate and anxiety levels in the Reiki group out of three groups that received Reiki, sham Reiki and standard care. In line with these studies, evidence-based data on the effectiveness of Reiki is thought to help nurses reduce patients' postoperative pain and anxiety, reduce the incidence of respiratory complications and help them evaluate and manage physiological parameters more accurately.

Status (registry)
Completed
Study type
Interventional
Enrollment
64 (actual)
First submitted
29 Aug 2024
Start date
10 Jul 2023
Primary completion date
26 Aug 2024
Lead sponsor
Istanbul University - Cerrahpasa
NCT number
NCT07175558

What you commit to

  • Study type: Interventional
  • Participants enrolled: 64
  • From 10 Jul 2023 to the primary completion date, 26 Aug 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • If a different surgical procedure is performed other than colorectal surgery,
  • If the patient has had abdominal surgery before,
  • If the patient has had reiki or energy therapies before,
  • If the patient is using medications other than the routine treatment after the surgery, the patients will be excluded from the study.

Other illness

  • If there is cancer pain,
  • If there are complex cancer metastases,
  • If there are secondary metastases from colorectal cancer,

Other

  • If the score determined in the Visual Comparison Scale in the pre-operative evaluation of the patient is 7 and above,
  • If there is persistent severe nausea and vomiting during the procedure and post-operative period,
  • If the patient is illiterate,
  • If the patient is over 50 points from the Trait Anxiety Scale,

Who the study is looking for

  • Patients who volunteer to participate and continue in the study,
  • Have no communication problems that would prevent the interview,
  • Have pain levels of 5 and above according to the GKO,
  • Have no history of psychiatric disorders and therefore do not use medication will be included in the study.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Haydarpaşa Numune Eğitim ve Araştırma Hastanesi
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.