Effectiveness of Group and Individual Training in EFT for Patients in Remission From Melanoma
1 other identifier
interventional
56
1 country
1
Brief Summary
Serious medical diagnosis frequently induce fear focused on specific anticipations or generalized anxiety, along with uncertainty, insecurity, and disorientation. Other emotions such as anger, depression, hopelessness, shame, or grief may also become involved following a serious diagnosis. The adverse impact of stress on health and immune function is well-established, as well as its link to depression and anxiety. Emotional Freedom Techniques (EFT) has demonstrated efficacy in treating anxiety, depression, and PTSD. This study tests its effectiveness in reducing negative emotional symptoms in general, and fear of recurrence in particular, among individuals previously diagnosed with melanoma and currently in remission.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Oct 2022
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 3, 2022
CompletedFirst Posted
Study publicly available on registry
June 16, 2022
CompletedStudy Start
First participant enrolled
October 20, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 20, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
July 20, 2025
CompletedApril 27, 2026
April 1, 2026
2.8 years
April 3, 2022
April 22, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
Illness perception
Change in score on Revised Illness Perception Questionnaire (IPQ-R)
Pre intervention, post 4 week intervention, and 3 month follow-up
Perception of recurrence
Change of perceived recurrence risk on a Likert scale
Pre intervention, post 4 week intervention, and 3 month follow-up
Secondary Outcomes (5)
Other physical symptoms
Pre intervention, post 4 week intervention, and 3 month follow-up
Depression
Pre intervention, post 4 week intervention, and 3 month follow-up
Anxiety
Pre intervention, post 4 week intervention, and 3 month follow-up
Patient's self-report of quality of life
Pre intervention, post 4 week intervention, and 3 month follow-up
Wellbeing
Pre intervention, post 4 week intervention, and 3 month follow-up
Study Arms (3)
Individual EFT Therapy
EXPERIMENTALPersonal EFT instruction and practice group
Group EFT Therapy
EXPERIMENTALGroup EFT instruction and practice group
Wait List
NO INTERVENTIONWait list control group
Interventions
EFT is an efficacious method demonstrated in over 100 clinical trials. It combines cognitive and exposure techniques with acupressure, in the form of fingertip percussion on acupuncture meridian points.
Eligibility Criteria
You may qualify if:
- Melanoma diagnosis over six months prior to the study; confirmed by clinical, dermoscopic examination and pathology results
You may not qualify if:
- In active treatment for melanoma
- schizophrenia
- epilepsy
- other malignant disease
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Soul Medicine Institutelead
- Tel Aviv Universitycollaborator
Study Sites (1)
The School Of Social Work Tel Aviv University
Tel Aviv, 69978, Israel
Related Publications (1)
Lazarov A, Church D, Shidlo N, Benyamini Y. The Effectiveness of Group and Individual Training in Emotional Freedom Techniques for Patients in Remission from Melanoma: A Randomized Controlled Trial. Healthcare (Basel). 2025 Jun 13;13(12):1420. doi: 10.3390/healthcare13121420.
PMID: 40565447RESULT
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Yael Benyamini, PhD
Tel Aviv University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Masking Details
- Participants in the two treatment arms, and data analysts, will be blind to group assignment.
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- SEQUENTIAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 3, 2022
First Posted
June 16, 2022
Study Start
October 20, 2022
Primary Completion
July 20, 2025
Study Completion
July 20, 2025
Last Updated
April 27, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will share
- Time Frame
- Data will be made available upon publication and for 5 years thereafter.
- Access Criteria
- Email request from qualified investigator.
An anonymized data file will be made available to any other qualified investigator who requests it.