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NCT04610151 Clinical Trial

The Effects of Guided Imagery on Postoperative Pain Management

Healthy Clinical Trial

Official title:
The Effects of Guided Imagery on Postoperative Pain Management: A Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04610151
Other study ID # LZA2018/5
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2018
Est. completion date September 30, 2018

Study information
Verified date October 2020
Source Dicle University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study was conducted to determine the effects of guided imagery on postoperative pain management.

Description:

The sample of the study consisted of 60 patients (30 in the experiment and 30 in the control groups) undergoing lower extremity operations at the orthopedics clinics of the Kahramanmaras Necip Fazil City Hospital. The study was conducted between April and September 2018.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date September 30, 2018
Est. primary completion date June 30, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Adult patients at and over the age of 18 - Patients who were able to speak Turkish - Patients who received spinal anesthesia Exclusion Criteria: - Patients who had not previously used guided imagery - Patients any disease that could cause pain outside the surgery

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• guided imagery
Guided Imagery CD: A guided imagery CD was prepared by a web designer with the recommendations of the researcher to include relaxing, soft and slow-paced, mixed nature sounds and photographs towards reducing pain in lower extremity surgical operation patients. The directives used for guidance, the audio recordings created as a result of literature review and the video lasted for 13 minutes (

Locations
Country Name City State
Turkey Leyla ZENGIN AYDIN Diyarbakir Sur

Sponsors (1)
Lead Sponsor Collaborator
Dicle University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary A mean total score on the Visual Analogue Scale (VAS) A mean total score on the VAS of four and above indicates postoperative pain. first week
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