NCT07193784

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
85

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jul 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 15, 2025

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

August 19, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

September 26, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 15, 2025

Completed
15 days until next milestone

Study Completion

Last participant's last visit for all outcomes

November 30, 2025

Completed
Last Updated

March 24, 2026

Status Verified

March 1, 2026

Enrollment Period

4 months

First QC Date

August 19, 2025

Last Update Submit

March 19, 2026

Conditions

Keywords

coronary angiographyreikipaincomfort

Outcome Measures

Primary Outcomes (1)

  • Pain level

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

    Baseline (before intervention), 30 minutes after intervention, 2 hours after intervention, and prior to first mobilization (within 24 hours).

Secondary Outcomes (1)

  • Comfort level

    Baseline (before intervention), 30 minutes after intervention, 2 hours after intervention, and prior to first mobilization (within 24 hours).

Study Arms (3)

Reiki

EXPERIMENTAL

Participants receive a 30-minute Reiki session by a trained practitioner after coronary angiography. Pain and comfort are assessed at four time points.

Behavioral: Reiki

Sham reiki

PLACEBO COMPARATOR

Participants receive a 30-minute sham Reiki session mimicking Reiki hand positions without actual energy intervention. Pain and comfort are assessed at the same time points.

Behavioral: Sham reiki

Control

NO INTERVENTION

Participants receive standard post-angiography care without any Reiki or sham intervention. Pain and comfort are assessed at the same time points.

Interventions

ReikiBEHAVIORAL

Reiki therapy applied by trained practitioner for 30 minutes.

Reiki
Sham reikiBEHAVIORAL

Sham Reiki applied by same practitioner, mimicking Reiki without actual energy technique.

Sham reiki

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Mersin University Hospital

Mersin, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Pain

Interventions

Therapeutic Touch

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Mind-Body TherapiesComplementary TherapiesTherapeuticsSpiritual Therapies

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Masking Details
Participants are blinded to their group allocation. Reiki and sham Reiki sessions are delivered in identical settings (duration, environment, body position, and practitioner interaction) to maintain blinding. Practitioners, who also serve as data collectors, are aware of the intervention type due to the nature of the technique. Statistical analysis will be performed by an independent researcher blinded to group allocation.
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Randomized, single-blind, placebo-controlled, parallel-group trial with three arms (Reiki, sham Reiki, and control). Participants are allocated in a 1:1:1 ratio and receive only the intervention assigned to their group. No crossover between arms is planned.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Abdullah Avcı, PhD, Principal Investigator, Nursing Services Coordinator, Mersin University Hospital

Study Record Dates

First Submitted

August 19, 2025

First Posted

September 26, 2025

Study Start

July 15, 2025

Primary Completion

November 15, 2025

Study Completion

November 30, 2025

Last Updated

March 24, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations