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Clinical Trials/NCT06853860
NCT06853860CompletedNot Applicable

Comparison of the Effects of Reflexology and Classical Hand Massage on Pain, Anxiety, and Vital Signs in Patients After Coronary Angiography

Kutahya Health Sciences University1 site in 1 country70 target enrollmentStarted: February 15, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
70
Locations
1
Primary Endpoint
Average Pain Score on Visual Analog Scale (VAS)

Study Overview

Brief Summary

There is no study finding examining the effects of the classical hand massage and hand reflexology massage methods on pain, anxiety and physiological parameters after coronary angiography. Therefore, the aim of this study is to examine the effects of reflexology hand massage and classical hand massage on pain, anxiety and physiological parameters after coronary angiography.

Detailed Description

There is no study finding examining the effects of the classical hand massage and hand reflexology massage methods on pain, anxiety and physiological parameters after coronary angiography.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Single (Outcomes Assessor)

Masking Description

Patients will be divided into experimental and control groups. Patients will know that they are participating in the study and the interventions that will be applied to them, but they will be blinded by not knowing which group they are in. The study data will be collected by a second researcher who is blinded to the groups. In the statistical analysis of the data, the groups will be labeled as group 1 and group 2, and the third researcher will be blinded when evaluating the results. Thus, the third researcher will be blinded to the study groups. In order to avoid bias in the evaluation of the results, the first researcher who is not blinded will not participate in any stage of the evaluation process.

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •• Patients who are over 18 years old
  • •Can speak Turkish
  • •Agree to participate in the study
  • •Have not undergone emergency coronary angiography
  • •Have not consumed coffee or hypnotic drugs at least 12 hours before
  • •Have no history of chronic pain (e.g. arthritis)
  • •Are not addicted to alcohol or drugs
  • •Have no psychological problems (such as depression, anxiety disorder)
  • •Have no problem with having their hands massaged; those who do not have any skin lesions, sensory and motor disorders, amputations, burns, or pathological diseases related to muscles and bones
  • •Have not used anxiolytics

Exclusion Criteria

  • •• Those who do not volunteer to participate in the study
  • •Those who have any skin lesions, burns, open wounds, muscle and bone pathological diseases on their hands,
  • •Those who develop delirium during the follow-up period
  • •Those who develop complications after coronary angiography (such as bleeding, etc.)
  • •Arrhythmia
  • •Hemodynamic instability

Arms & Interventions

reflexology group

Experimental

reflexology group

Intervention: reflexology massage (Other)

Classic hand massage group

Placebo Comparator

Classic hand massage group

Intervention: classic hand massage (Other)

Outcomes

Primary Outcomes

Average Pain Score on Visual Analog Scale (VAS)

Time Frame: 0 hour (baseline), 1st hour, 2nd hour, 3rd hour

Pain will be measured using the Visual Analog Scale (VAS), ranging from 0 (no pain) to 10 (severe pain). Higher scores indicate more severe pain.

State Anxiety Scale Mean Score

Time Frame: 0 hour (baseline), 1st hour, 2nd hour, 3rd hour

Anxiety will be measured using the State Anxiety Scale, a validated questionnaire assessing current anxiety levels. Higher scores indicate higher levels of anxiety.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Kutahya Health Sciences University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Necibe Dağcan

Assistant Professor of Nursing

Kutahya Health Sciences University

Study Sites (1)

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