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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05887362
Other study ID # 2022935
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2022
Est. completion date November 15, 2022

Study information

Verified date June 2023
Source Alexandria University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Reflexology influences pain perception and pain-impulse transmission by releasing endorphins (12). Patients with a variety of medical illnesses can benefit from hand reflexology by lessening their physical and emotional discomfort (13, 14). Therefore, this study was done to investigate the power of hand reflexology in ameliorating anxiety, pain, and fatigue among patients undergoing coronary angiography


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date November 15, 2022
Est. primary completion date November 1, 2022
Accepts healthy volunteers No
Gender All
Age group 20 Years to 60 Years
Eligibility Criteria: Inclusion Criteria: - Patients between the ages of 20 and 60 who were scheduled for non-emergency CA, Absence of any hands' sensory motor disorders, or upper limb vascular injuries. - No abnormalities such as amputations, burns, skin lesions, and intervertebral disc herniation. - No history of mental illnesses. Exclusion Criteria: Patients with severe mental problems

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Hand Reflexology
Reflexology is a well-known, safe, and noninvasive alternative medicine technique. It alludes to a treatment that is applied to particular areas of the hands and feet. The compression on the hands or feet serves as a sensor linked to particular body areas. These sensors are activated by the reflexology technique to improve blood flow, energize, relax, and maintain homeostasis.

Locations

Country Name City State
Egypt Faculty of Nursing, Alexandria university Alexandria

Sponsors (1)

Lead Sponsor Collaborator
Alexandria University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain intensity It is a 10 cm horizontal line with two ends; the left end typically denotes "no pain," while the right end typically denotes "worst possible pain." 4 months
Primary Fatigue The Rhoten Fatigue Scale (RFS) is a subjective rating scale developed by (16) to measure a patient's fatigue level. It comprises a 10-centimeter line with extremely positive and negative statements at either end. 4 months
Primary Anxiety The Beck Anxiety Inventory (BAI) was developed in 1988 by (17) to assess the severity of anxiety symptoms. The Likert scale for the 21 items that comprise the BAI ranges from 0 to 3. The overall score is between 0 and 63. 4 months
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