NCT05216783 is a NA clinical trial of Motivational Interviews in Trauma, sponsored by Inonu University.

Who is sponsoring NCT05216783?

NCT05216783 is sponsored by Inonu University.

What drugs are being tested in NCT05216783?

Interventions in NCT05216783: Motivational Interviews.

What condition does NCT05216783 study?

NCT05216783 studies Trauma, Childbirth, Self Efficacy.

Is NCT05216783 still recruiting?

NCT05216783 is currently completed. Last updated 1 February 2022.

Last reviewed 2022-02-01 · How we verify

NCT05216783

Name: Drug Landscape Pharmaceutical Database
Creator: Drug Landscape
Published: 2026-01-01
License: https://creativecommons.org/licenses/by/4.0/

Effect of Motivational Interviews on Childbirth Perception and Childbirth Self-Efficacy

Completed NA Last updated 1 February 2022

What this trial tests

NA trial testing Motivational Interviews in Trauma in 166 participants. Completed in 12 February 2021.

Timeline

12 November 2019

Primary endpoint
1 November 2020

12 February 2021

Quick facts

Lead sponsor	Inonu University
Phase	NA
Status	Completed
Study type	INTERVENTIONAL
Allocation	randomized
Design	crossover
Masking	single
Primary purpose	health services research
Enrollment	166
Start date	12 November 2019
Primary completion	1 November 2020
Estimated completion	12 February 2021
Sites	1 location across Turkey (Türkiye)

Drugs / interventions tested

Motivational Interviews

Conditions studied

Trauma — all drugs for Trauma →
Childbirth — all drugs for Childbirth →
Self Efficacy — all drugs for Self Efficacy →

Sponsor

Inonu University

Who can join

Adults 28 Weeks to 36 Weeks, female only, with Trauma or Childbirth. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Aim: The aim of this study to determine the effect of motivational interviews on the perception and self-efficacy of birth in nullipars with a perception of traumatic birth. Materials and Methods: The study was conducted in a randomized controlled, between November 2019 and November 2020 in the obstetrics outpatient clinics of Elazig Fethi Sekin City Hospital. In the power analysis, the sample size was calculated as at least 83 pregnant women for each group (83 experiment, 83 control). Data were collected with Descriptive Information Form, Traumatic Childbirth Perceptions Scale (TCPS) and Childbirth of Self-Efficacy Scale-Short From (CBSE). Pregnant women in the experimental group were held with four sessions of motivational interviews one week a part. No intervention was made for the pregnant women in the control group. Descriptive statistics, chi-square test, t test for dependent and independent groups were used in data analysis

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

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Other Inonu University trials

Trials by the same sponsor.

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Verify against primary sources

ClinicalTrials.gov — authoritative US registry record
WHO ICTRP — international registry index
EU Clinical Trials Register
Sponsor press releases (Google)

Data sources for this page

Trial protocol + status: ClinicalTrials.gov NCT05216783 (US National Library of Medicine, public domain)
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by Inonu University
Last refreshed: 1 February 2022

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05216783.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing