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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06440109
Other study ID # A-TURAN-001
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 30, 2024
Est. completion date September 30, 2024

Study information

Verified date May 2024
Source KTO Karatay University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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. The research will be conducted between November 2023 and November 2024 with women who gave birth normally and are registered at Karakulak Family Health Center in Konya. 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. A pilot study was conducted with 15 people to calculate the sample size. The number of samples was determined as 60 by post hoct analysis in the G*Power 3.1.9.4 program, in line with the pilot study results. Data will be collected with the Personal Information Form, Brief Mood Introspection Scale, Visual Similarity Scale for Fatigue, and Unit of Subjective Experience (SUE). The analysis of the data obtained from the research will be carried out in the Social Sciences Statistical Package (SPSS) 25.0 package program. The critical significance value will be taken as 0.05. Therapeutic touch and EFT interventions are thought to be methods that can be used to improve women's health because they are easy to apply, have no side effects, and are non-drug practices that midwives/nurses can apply independently.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date September 30, 2024
Est. primary completion date September 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - 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 Exclusion Criteria: - 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.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Emotional freedom technique (EFT)
Intervention groups will be followed for six months and one of the six EFT therapies will be applied, one session every week.
Therapeutic touch (TD)
Intervention groups will be followed for six months and one of the six TD therapies will be applied, one session every week.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
KTO Karatay University

Outcome

Type Measure Description Time frame Safety issue
Primary Postpartum 3rd-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
Primary 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
Primary 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
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