NCT07119554

Brief Summary

With the acceleration of developments in health technology, changes have occurred in professional knowledge and practices, as well as in patient needs and expectations. These changes have also influenced the way nursing care is delivered, leading to a shift from traditionally applied training methods to more modern and technology-based education tools. These include telephone counseling, online and web-based counseling, and the use of models. In recent years, the use of motivational interviewing techniques in providing counseling services has become increasingly common in the field of nursing and is considered an effective communication method. In light of this information, the aim of this study is to evaluate the effect of postpartum contraceptive counseling based on the Health Belief Model using motivational interviewing techniques, along with spousal participation, on women's attitudes toward family planning and their intention to use contraceptives.

Trial Health

75
On Track

Trial Health Score

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

Enrollment
62

participants targeted

Target at P50-P75 for not_applicable

Timeline
3mo left

Started Jul 2025

Geographic Reach
1 country

1 active site

Status
active not recruiting

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

Study Progress77%
Jul 2025Sep 2026

Study Start

First participant enrolled

July 1, 2025

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

August 5, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

August 13, 2025

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2026

Completed
9 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2026

Expected
Last Updated

August 13, 2025

Status Verified

August 1, 2025

Enrollment Period

6 months

First QC Date

August 5, 2025

Last Update Submit

August 12, 2025

Conditions

Keywords

PostpartumRegulation of fertilityContraceptionMotivational interviewing

Outcome Measures

Primary Outcomes (1)

  • Change from baseline in attitudes toward family planning and contraceptive method use intention scale scores at 6 months

    Postpartum contraceptive method counseling provided through motivational interviewing based on the health belief model

    in the 6th months after birth

Study Arms (2)

HBM-Based Counselling Group

EXPERIMENTAL

Participants in this group will receive individual contraceptive counselling based on the Health Belief Model (HBM) from the first month after birth until the sixth month.

Behavioral: HBM-Based Postpartum Contraceptive Counselling

Standard care group

NO INTERVENTION

Participants in this group will receive only routine care provided by health facilities, without any structured contraceptive counselling during the postpartum period.

Interventions

This intervention involves providing a structured, individual contraceptive counseling session based on the Health Belief Model (HBM) to women in the postpartum period.The session is delivered face-to-face, lasts approximately 30 to 45 minutes, and is structured around the core components of the HBM: perceived susceptibility, perceived severity, perceived benefits, perceived barriers, self-efficacy, and cues to action. The aim of the intervention is to improve attitudes toward family planning and increase the intention to use contraceptive methods.

HBM-Based Counselling Group

Eligibility Criteria

Age18 Years+
Sexfemale(Gender-based eligibility)
Gender Eligibility Detailsfemale gender
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Women who volunteered to participate in the study,
  • were 18 years of age or older,
  • were primiparous,
  • spoke Turkish,
  • owned a smartphone,
  • had no chronic illness or diagnosed mental or psychiatric illness, were included in the study.

You may not qualify if:

  • Women whose partners have undergone or will undergo a vasectomy, and women who have chosen tubal ligation will not be included in the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Health Sciences, Hamidiye Institute of Health Sciences

Istanbul, Turkey (Türkiye)

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: A randomised controlled trial using motivational interviewing in two groups
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

August 5, 2025

First Posted

August 13, 2025

Study Start

July 1, 2025

Primary Completion

January 1, 2026

Study Completion (Estimated)

September 30, 2026

Last Updated

August 13, 2025

Record last verified: 2025-08

Locations