Effect of Motivational Counseling on the Intention to Use Modern Contraceptive Methods

NCT ID: NCT07184229

Last Updated: 2025-09-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-09-16

Study Completion Date

2025-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The motivational interviewing process consisted of 5 stages with 8 participants per group. A pre-interview will be conducted, followed by the first session one week later. The remaining four sessions will be held at two-week intervals, for a total duration of 9 weeks. The first and last sessions lasted 60 minutes; the others about 45 minutes. The stages of the motivational interviews were planned as follows:

Initial Session: Purpose and process explained, participant experiences assessed, and pre-tests conducted.

Engagement: Explored feelings and experiences about traditional family planning methods.

Supporting Self-Efficacy: Evaluated knowledge and confidence in modern methods. Change Talk: Focused on motivation and awareness for switching to modern methods.

Planning and Maintenance: Concrete action plans created, barriers and coping strategies discussed, and post-tests administered at the end.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Contraception

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

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.
Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Participants

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Family planning

Standard family planning counseling

Group Type ACTIVE_COMPARATOR

standard family planning counseling.

Intervention Type BEHAVIORAL

The comparator group will receive only standard family planning counseling.

Control

No intervention

Group Type NO_INTERVENTION

No interventions assigned to this group

Motivational Interviewing

Motivational interviewing-based family planning counseling

Group Type EXPERIMENTAL

motivational interviewing-based family planning counseling

Intervention Type BEHAVIORAL

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.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

motivational interviewing-based family planning counseling

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.

Intervention Type BEHAVIORAL

standard family planning counseling.

The comparator group will receive only standard family planning counseling.

Intervention Type BEHAVIORAL

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

standard family planning counseling

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

Women aged between 18 and 49 years

* Literate in Turkish
* Currently using a traditional family planning method (e.g., withdrawal method)

Exclusion Criteria

* Diagnosed psychiatric disorder
* Currently pregnant
Minimum Eligible Age

18 Years

Maximum Eligible Age

49 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Adiyaman University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Çiğdem Erdemoğlu

Dr

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

K-8 Containerkent

Adıyaman, , Turkey (Türkiye)

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Çiğdem Erdemoğlu, Dr

Role: CONTACT

095385076024

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Çiğdem Erdemoğlu, Dr

Role: primary

0905385076024

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2024/9-19

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Video Intervention Fertility Awareness Training
NCT06541717 NOT_YET_RECRUITING NA