The Effect of Therapeutic Touch and Emotional Freedom Technique on Postpartum Mood and Fatigue in Postpartum Women
1 other identifier
interventional
60
1 country
1
Brief Summary
Therapeutic touch (TD) is a non-pharmacological/integrated treatment method used to balance the body by regulating the imbalanced energy field in the individual or resolving blockages in energy flow. Emotional freedom technique (EFT) is a psychophysiological intervention that combines elements of somatic stimulation using acupuncture points. This research will be conducted as a randomized controlled experimental study to determine the effect of TD and EFT intervention on postpartum mood and fatigue in postpartum women. This study is planned to be conducted between April 2024 and June 2025 with postpartum women who meet the inclusion criteria and who apply to the Obstetrics and Gynecology Clinic of Necmettin Erbakan University Faculty of Medicine Hospital. This research; It was planned to be carried out with three groups: TD intervention, EFT intervention and control group. The population of the research consists of women who gave birth vaginally and those who gave birth vaginally in the relevant hospital.
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 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 8, 2024
CompletedFirst Posted
Study publicly available on registry
June 3, 2024
CompletedStudy Start
First participant enrolled
October 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
June 10, 2025
CompletedSeptember 12, 2025
March 1, 2024
8 months
May 8, 2024
September 6, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Postpartum 1rd-5th. EFT intervention will be applied to women who are between
SUE scale and vital signs will be taken from the participants before and after each session.
six weeks
Postpartum 3rd-5th. TD intervention will be applied to women who are between
SUE scale and vital signs will be taken from the participants before and after each session.
six weeks
3rd-5th postpartum Pre- and post-test will be given to women between
The researcher will not perform any intervention on women in this group. After the pre-tests are completed, women in this group will be called by phone during the interview weeks for the intervention group, their postpartum needs will be questioned and support will be provided when necessary. The implementation of the final tests will be completed in the sixth week.
six weeks
Study Arms (3)
EFT intervention
EXPERIMENTALThe application will be carried out in line with EFT application protocols. In this regard, women's home visits will be completed with 6 meetings, once every week. Each EFT session will last 15 minutes
TD intervention
EXPERIMENTALThe application will be carried out in line with TD application protocols. In this regard, women's home visits will be completed with 6 meetings, once every week. Each TD session will last 15 minutes
Control grup
NO INTERVENTIONNo intervention will be made. Women in the intervention groups will be followed for 6 weeks and receive standard care. The final test will be administered at the end of the sixth week
Interventions
İntervention groups will be followed for six months and one of the six EFT therapies will be applied, one session every week.
İntervention groups will be followed for six weeks and one of the six TD therapies will be applied, one session every week.
Eligibility Criteria
You may qualify if:
- Having a vaginal birth at term
- Being primiparous
- Postpartum 3rd-5th. to be in the days
- Being able to speak and understand Turkish
- Being 18 years or older
- Having a single and viable fetus
- Volunteering to participate in research
- Not having experienced TD or EFT treatment before
You may not qualify if:
- A psychiatric diagnosis has been made,
- Having a chronic systemic disease,
- The newborn's need for treatment
- Having postpartum complications in the mother or baby
- Those who have sensitivity or problems with touch,
- Wounds, infections, etc. in places that need to be touched. existence of situations,
- Women who have any disability that would prevent communication (deafness, hearing impairment, etc., use of languages other than Turkish) will be excluded from the research.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
KTO Karatay University
Karatay, Konya, 42020, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Aslıhan Turan, PhD (c)
KTO Karatay University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 8, 2024
First Posted
June 3, 2024
Study Start
October 1, 2024
Primary Completion
June 1, 2025
Study Completion
June 10, 2025
Last Updated
September 12, 2025
Record last verified: 2024-03
Data Sharing
- IPD Sharing
- Will not share