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Coronary AngiographyNCT07193784

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

A study testing Reiki in people with Coronary Angiography, run by Mersin University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 to 80 years
Conditions the study is for
Coronary Angiography
What is being tested?
Reiki
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
85 participants
Where
1 siteTurkey (Türkiye)
Study dates
15 Jul 2025to 30 Nov 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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.

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Mersin University Hospital

    Mersin

Other trials in Turkey (Türkiye)

About this study

Official title: Effect of Reiki Applied After Coronary Angiography on Pain and Comfort Level: A Randomized Single-blind Placebo-controlled Study

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.

Read the detailed description

This study is a randomized, single-blind, placebo-controlled trial designed to evaluate the effect of Reiki therapy on pain and comfort levels in patients undergoing coronary angiography. Participants are randomly assigned to one of three groups: Reiki intervention, sham Reiki, or control group.

The Reiki intervention is administered by a trained practitioner for approximately 21-30 minutes following the procedure, focusing on standard energy points. The sham Reiki group receives a similar procedure without therapeutic intent, while the control group receives standard care only.

Pain levels are assessed using the Visual Analog Scale (VAS), and comfort levels are measured using the General Comfort Scale Short Form. Measurements are conducted at baseline and at specified intervals following the intervention.

The study aims to provide evidence regarding the effectiveness of Reiki as a complementary, non-pharmacological intervention in post-procedural nursing care.

Being tested
Reiki, Sham reiki
Keywords
coronary angiography, reiki, pain, comfort
Medical subject headings
Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ReikiBehavioural

    Reiki therapy applied by trained practitioner for 30 minutes.

  • Sham reikiBehavioural

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

Study groups in NCT07193784
Study groupRoleWhat they receive
ReikiExperimentalParticipants receive a 30-minute Reiki session by a trained practitioner after coronary angiography. Pain and comfort are assessed at four time points.
Receives: Behavioral: Reiki
Sham reikiPlacebo comparatorParticipants 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.
Receives: Behavioral: Sham reiki
ControlNo interventionParticipants receive standard post-angiography care without any Reiki or sham intervention. Pain and comfort are assessed at the same time points.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pain level

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

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

Secondary outcomes (1)
  1. Comfort level

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

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

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Sep 2025
  2. Study start15 Jul 2025
  3. Primary completion15 Nov 2025
  4. Study completion30 Nov 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
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.
Masking
Single blind
Who is masked
Participant
Enrolment
85 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07193784
Sponsor's protocol ID
AVCI-MERSİN-2025
Status last verified
Mar 2026
First submitted
19 Aug 2025
Last updated
24 Mar 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Reiki in people with Coronary Angiography, run by Mersin University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 24 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Pain level (time frame: Baseline (before intervention), 30 minutes after intervention, 2 hours after intervention, and prior to first mobilization (within 24 hours).). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Mar 2026.

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