NCT06440109

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Oct 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
26 days until next milestone

First Posted

Study publicly available on registry

June 3, 2024

Completed
4 months until next milestone

Study Start

First participant enrolled

October 1, 2024

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2025

Completed
9 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 10, 2025

Completed
Last Updated

September 12, 2025

Status Verified

March 1, 2024

Enrollment Period

8 months

First QC Date

May 8, 2024

Last Update Submit

September 6, 2025

Conditions

Keywords

emotional freedom technictherapeutic touchfatiguemood state level

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

EXPERIMENTAL

The 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

Other: Emotional freedom technique (EFT)

TD intervention

EXPERIMENTAL

The 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

Other: Therapeutic touch (TD)

Control grup

NO INTERVENTION

No 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.

EFT intervention

İntervention groups will be followed for six weeks and one of the six TD therapies will be applied, one session every week.

TD intervention

Eligibility Criteria

Age18 Years - 60 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

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)

Location

MeSH Terms

Conditions

FatigueEmotional Regulation

Interventions

Therapeutic Touch

Condition Hierarchy (Ancestors)

Signs and SymptomsPathological Conditions, Signs and SymptomsSelf-ControlSocial BehaviorBehavior

Intervention Hierarchy (Ancestors)

Mind-Body TherapiesComplementary TherapiesTherapeuticsSpiritual Therapies

Study Officials

  • Aslıhan Turan, PhD (c)

    KTO Karatay University

    PRINCIPAL INVESTIGATOR

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

Locations