NCT07184229

Brief Summary

This study aims to evaluate the effect of motivational interviewing-based family planning counseling on attitudes and intentions toward modern contraceptive methods among women currently using traditional contraceptive methods. Despite the widespread use of traditional methods in many regions, including Turkey, modern contraceptive methods remain underutilized, leading to increased unintended pregnancies and related health burdens. Motivational interviewing is a client-centered counseling approach that supports individuals in making informed health decisions. By providing tailored counseling, this study seeks to improve women's awareness and motivation to adopt effective modern contraceptive methods, ultimately enhancing reproductive health outcomes. The findings are expected to contribute valuable insights for healthcare providers to improve family planning services and support women's reproductive choices.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
120

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Sep 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet 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

First Submitted

Initial submission to the registry

September 14, 2025

Completed
2 days until next milestone

Study Start

First participant enrolled

September 16, 2025

Completed
3 days until next milestone

First Posted

Study publicly available on registry

September 19, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 30, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2025

Completed
Last Updated

September 25, 2025

Status Verified

September 1, 2025

Enrollment Period

3 months

First QC Date

September 14, 2025

Last Update Submit

September 20, 2025

Conditions

Keywords

traditional contraceptive methodsfamily planningmotivational interviewingwomen

Outcome Measures

Primary Outcomes (1)

  • Change in attitude toward modern contraceptive methods

    Assessed using a validated scale measuring women's attitudes toward modern contraceptive methods. Family Planning Attitude Scale: The scale was developed by Örsal and Kubilay in 2007. It is a 5-point Likert-type scale consisting of 34 items. Each statement on the scale is scored as "1=Strongly Agree," "2=Agree," "3=Undecided," "4=Disagree," and "5=Strongly Disagree." The scale has three subdimensions: attitudes toward family planning in society (items 1-15), attitudes toward family planning methods (items 16-26), and attitudes toward childbirth (items 27-34). The attitude toward family planning in society subdimension scores range from 15 to 75, the attitude toward family planning methods subdimension scores range from 11 to 55, the attitude toward childbirth subdimension scores range from 8 to 40, and the total scale score ranges from 34 to 170. As the score on the scale increases, the attitude toward family planning becomes more positive.

    Before the intervention and 9 weeks post-intervention

Secondary Outcomes (1)

  • Change in intention toward modern contraceptive methods

    Before the intervention and 9 weeks post-intervention

Study Arms (3)

Family planning

ACTIVE COMPARATOR

Standard family planning counseling

Behavioral: standard family planning counseling.

Control

NO INTERVENTION

No intervention

Motivational Interviewing

EXPERIMENTAL

Motivational interviewing-based family planning counseling

Behavioral: motivational interviewing-based family planning counseling

Interventions

This intervention consists of motivational interviewing-based family planning counseling aimed at women currently using traditional contraceptive methods. The counseling sessions are designed to enhance participants' motivation and readiness to adopt modern contraceptive methods by addressing their concerns, increasing knowledge, and resolving ambivalence. The comparator group will receive only standard family planning counseling.

Also known as: standard family planning counseling
Motivational Interviewing

The comparator group will receive only standard family planning counseling.

Family planning

Eligibility Criteria

Age18 Years - 49 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Women aged between 18 and 49 years
  • Literate in Turkish
  • Currently using a traditional family planning method (e.g., withdrawal method)

You may not qualify if:

  • Diagnosed psychiatric disorder
  • Currently pregnant

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

K-8 Containerkent

Adıyaman, 02000, Turkey (Türkiye)

Location

Central Study Contacts

Çiğdem Erdemoğlu, Dr

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: The study will include a total of 120 women, consisting of two control groups and one intervention group, each with 40 participants. The intervention group will receive motivational interviewing-based family planning counseling, the control group 1 will receive standard family planning counseling, and the control group 2 will receive no intervention.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr

Study Record Dates

First Submitted

September 14, 2025

First Posted

September 19, 2025

Study Start

September 16, 2025

Primary Completion

November 30, 2025

Study Completion

December 31, 2025

Last Updated

September 25, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will share

Demographic data and survey results, with all personal identifiers removed, will be shared with researchers at the time of publication.

Time Frame
IPD will be available starting 6 months after publication and will remain accessible for 3 years.
Access Criteria
Access will be granted to qualified researchers upon reasonable request and after approval by an independent review committee.

Locations