The Effect Of Reflexology On Pain, Anxiety And Comfort Level

Sponsor
Hakkari Universitesi (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT06007716
Collaborator
(none)
74
1
2
27
2.7

Study Details

Study Description

Brief Summary

This study was performed as a randomized controlled a study with a pre test-post test design, aimed to determine affect of reflexology masagge to the pain, anxiety and comfort level on the patients that are percutaneous coronary intervention.

Condition or Disease Intervention/Treatment Phase
  • Other: reflexology massage
  • Other: Placebo massage
N/A

Detailed Description

A total of 74 patients, 37 in the experimental group and 37 in the placebo group, who met the criteria for inclusion in the study, constituted the sample of the study. Research data were collected with "Structured Patient Information Form", "Vital Signs Form", "State Anxiety Scale", "Visual Comparison Scale", "McGill Pain Scale Short Form" and "General Comfort Scale Short Form". Appropriate statistical methods were used in the analysis of the data.

Reflexology massage is a well tolerated, inexpensive, applicable and safe non-pharmacological method. The fact that nurses are educated and experienced about reflexology massage is of great importance for integrating reflexology massage into clinical settings.

If the results of this study are significant, it will be concluded that reflexology massage is effective in the management of pain and anxiety and increasing the comfort level in patients undergoing PCI. It will be recommended that reflexology massage be used in clinics to reduce pain, anxiety and increase comfort level in individuals undergoing PCI, and to include it in patient education. No study has been found in the national literature evaluating the effectiveness of reflexology massage in the management of PCI-related pain, anxiety and comfort. It is thought that this study will fill an important gap in the literature. The aim of this study, carried out in this context, is to reveal the effect of reflexology massage on pain, anxiety and comfort level in patients undergoing PCI.

Study Design

Study Type:
Interventional
Actual Enrollment :
74 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
consists of experimental and placebo groups.consists of experimental and placebo groups.
Masking:
Single (Participant)
Masking Description:
Participants were informed about the study after obtaining an informed consent form. It was noted that the participants had not received reflexology or classical massage before.
Primary Purpose:
Supportive Care
Official Title:
The Effect Of Reflexology Massage On Pain, Anxiety And Comfort Level In Patients Undergoing Percutaneous Coronary Intervention
Actual Study Start Date :
Jul 1, 2021
Actual Primary Completion Date :
Feb 27, 2022
Anticipated Study Completion Date :
Sep 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Experimental group

it was planned to apply reflexology massage once a day for each patient for 2 consecutive days, in total 2 sessions.

Other: reflexology massage
5 minutes of classic message on the left foot, 15 minutes of reflexology message, and 5 minutes of classic message on the right foot, 15 minutes of reflexology message, a total of 40 minutes of massage. 30 minutes after the massage, evaluation was recorded with the Vital Signs Registration Form, McGill Pain Scale Short Form, State Anxiety Inventory, General Comfort Scale Short Form, and Fatigue and Quality Sleep Visual Comparison Scale. Thus, reflexology massage is performed once a day for each patient for 2 consecutive days, for a total of 2 sessions.

Placebo Comparator: placebo group

placebo massage was applied once a day for each patient for 2 consecutive days, for a total of 2 sessions.

Other: Placebo massage
Placebo reflexology massage was applied to each foot for 20 minutes, for a total of 40 minutes.30 minutes after the massage, evaluation was recorded with the Vital Signs Registration Form, McGill Pain Scale Short Form, State Anxiety Inventory, General Comfort Scale Short Form, and Fatigue and Quality Sleep Visual Comparison Scale. Thus, Placebo massage is performed once a day for each patient for 2 consecutive days, for a total of 2 sessions.

Outcome Measures

Primary Outcome Measures

  1. The McGill Pain Scale Short Form-2 [2 days]

    The McGill Pain Scale Short Form, developed by Melzack in 1987, provides information about the sensory characteristics, severity and effect of pain. The validity and reliability study in Turkey was developed by Yakut et al. in 2007. McGill Pain Scale Short Form-2 (MAS-SF-2) was developed in 2010 by revising the McGill Pain Scale Short Form by Bicici and Günes.

Secondary Outcome Measures

  1. State-Trait Anxiety Inventory [2 days]

    It was developed by Spielberger et al. in 1970 and validated and reliable in Turkish society by Öner and Le Compte (1977). The State-Trait Anxiety Inventory consists of two different parts and includes a total of 40 items, 20 of which are each.

Other Outcome Measures

  1. General Comfort Scale Short Form [2 days]

    General Comfort Scale Short Form GQS-SF was developed by Kolcaba in 2006. Validity and reliability were established by Saritas et al. in 2018. It includes the sub-dimensions of comfort, relief (9 items), relaxation (9 items), and overcoming problems (10 items).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Over 18 years old,

  • Literate, Diagnosed with PCI-related pain,

  • Pain score of 4 out of 10 according to Visual Comparison Scale (VAS) after PCI.

Exclusion Criteria:
  • Presence of a pacemaker,

  • Having a diagnosis of diabetic foot,

  • Presence of vision, hearing, cognitive ability impairment or psychosis,

  • Being pregnant,

  • Presence of disc herniation,

  • Any contagious skin disease (shingles, fungus, etc.), open lesion/wound on the lower extremities, scar tissue, fracture, dislocation, amputation, edema, hematoma, thrombophlebitis, inflammatory and degenerative joint disease,

  • Having applied reflexology massage in the last month

Contacts and Locations

Locations

Site City State Country Postal Code
1 Van Regional Training and Research Hospital Van Turkey 65100

Sponsors and Collaborators

  • Hakkari Universitesi

Investigators

  • Principal Investigator: Kamber SÜMER, PhD student

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Kamber Sumer, Assistant professor, Hakkari Universitesi
ClinicalTrials.gov Identifier:
NCT06007716
Other Study ID Numbers:
  • HU-SM-KM-01
First Posted:
Aug 23, 2023
Last Update Posted:
Aug 23, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 23, 2023