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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06391268
Other study ID # FCetinkaya
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date January 3, 2022
Est. completion date June 28, 2024

Study information

Verified date April 2024
Source Ege University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The main aim of the study was to investigate self-administered emotional to determine the effect of the freedom technique on pain and stress levels. The sub-objectives of the study are as follows: 1. To determine the effect of self-administration of EFT on pain level. 2. To determine the effect of self-administered EFT on stress level. 3. To determine the effect of EFT self-administration on comfort level.


Description:

HYPOTHESES OF THE RESEARCH H 1 : Between the pain levels of patients with and without self-administered EFT there is a difference. H 2 : There is a difference between the stress levels of patients who apply EFT to themselves and those who do not. there is a difference. H 3 : Comfort levels of patients with and without self-administered EFT there is a difference.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 80
Est. completion date June 28, 2024
Est. primary completion date August 16, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Clinical diagnosis of fibromyalgia - Can speak and understand Turkish - Have time and place orientation - No psychiatric illness, - No vision and hearing problems. Exclusion Criteria: - Unstable medical condition - Non-cooperative individuals

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Emotional Freedom Technique (EFT) works on cognitive and energetic levels.
Emotional Freedom Technique (EFT) works on cognitive and energetic levels.

Locations

Country Name City State
Turkey Izmir Buca Seyfi Demirsoy Training and Research Hospital Izmir

Sponsors (2)

Lead Sponsor Collaborator
Ege University Buca Seyfi Demirsoy State Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Comparison of the self-EFT group Comparison of the group to which EFT was performed by the researcher, Brief Scan for Stress and Problem List to assess stress and problems (Calculated out of 10 points, cut-off point is 4), Brief Pain Invertory to assess pain: The numeric pain scale is evaluated on a scale of 0-10, with "0" representing no pain and "10" representing excruciating pain. Each item is rated on a numerical scale from 0 to 10; "0" means not affected at all, "100" means completely affected).
At the end of the study, pain and stress scores of the two experimental groups (EFT performed by the researcher and self-administered EFT) before and after EFT were analyzed and compared.
up to 24 weeks
Secondary Control grouup Comparison of the control group with other experimental groups, Comparison of the group to which EFT was performed by the researcher, Brief Scan for Stress and Problem List to assess stress and problems (Calculated out of 10 points, cut-off point is 4), Brief Pain Invertory to assess pain: The numeric pain scale is evaluated on a scale of 0-10, with "0" representing no pain and "10" representing excruciating pain. Each item is rated on a numerical scale from 0 to 10; "0" means not affected at all, "100" means completely affected).
Pain, comfort, fibromyalgia effect scale scores were calculated in the control group and compared with the experimental groups.
up to 24 weeks
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