NCT07540962

Brief Summary

This research was conducted to determine the effect of a motivational interview-based nursing care program on health beliefs and cancer fears related to cervical cancer and screening in rural women.

Trial Health

65
Monitor

Trial Health Score

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

Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
2mo left

Started Jun 2026

Shorter than P25 for not_applicable

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

March 31, 2026

Completed
21 days until next milestone

First Posted

Study publicly available on registry

April 21, 2026

Completed
2 months until next milestone

Study Start

First participant enrolled

June 27, 2026

Expected
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 2, 2026

1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

September 2, 2026

Last Updated

April 21, 2026

Status Verified

April 1, 2026

Enrollment Period

1 month

First QC Date

March 31, 2026

Last Update Submit

April 17, 2026

Conditions

Keywords

CERVICAL CANCERFEARCANCER SCREENINGMOTIVATIONAL INTERVIEW

Outcome Measures

Primary Outcomes (3)

  • Effect of motivational interviewing on health beliefs regarding cervical cancer and Pap smear

    Health beliefs will be assessed using the Cervical Cancer and Pap Smear Test Health Belief Model Scale.

    From baseline to 4 weeks

  • power calcilation

    "The sample size was calculated based on an effect size of 0.794, with 95% power and α=0.05. n:80"

    from registration until the end of the 4-week period

  • Effect of motivational interviewing on cancer anxiety

    Cancer anxiety will be measured using the Cancer Anxiety Scale.

    From baseline to 4 weeks

Study Arms (2)

Motivational Interviewing

EXPERIMENTAL

The motivational interviewing group will receive a total of four Motivational Interviewing-Based Nursing Care Programs, with women receiving one program per week. The control group will receive no intervention.

Behavioral: motivational interview

control

EXPERIMENTAL

No intervention will be made against the control group.

Behavioral: motivational interview

Interventions

A total of four motivational meetings, one per week.

Motivational Interviewingcontrol

Eligibility Criteria

Age30 Years - 65 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsThe woman must live in a rural area and be within the national cervical cancer screening range of 30-65 years.
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • The individual must be registered with the Sivaslı Community Health Center affiliated with the Uşak Provincial Health Directorate
  • Reside in a rural area
  • Be within the age range (30-65) suitable for the national screening program
  • Have an intellectual disability.

You may not qualify if:

  • Having a condition that prevents communication (unable to speak or understand Turkish, having a speech disorder)
  • being illiterate.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Links

MeSH Terms

Conditions

Uterine Cervical Neoplasms

Interventions

Motivational Interviewing

Condition Hierarchy (Ancestors)

Uterine NeoplasmsGenital Neoplasms, FemaleUrogenital NeoplasmsNeoplasms by SiteNeoplasmsUterine Cervical DiseasesUterine DiseasesGenital Diseases, FemaleFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesGenital Diseases

Intervention Hierarchy (Ancestors)

Directive CounselingCounselingMental Health ServicesBehavioral Disciplines and ActivitiesHealth ServicesHealth Care Facilities Workforce and Services

Study Officials

  • Öznur KÖRÜKCÜ, PROFESSOR

    Akdeniz University

    STUDY DIRECTOR

Central Study Contacts

Özge ASLAN KOYUTÜRK, doctoral student

CONTACT

Öznur KÖRÜKCÜ, PROFESSOR

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
SCREENING
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
doctoral student

Study Record Dates

First Submitted

March 31, 2026

First Posted

April 21, 2026

Study Start (Estimated)

June 27, 2026

Primary Completion (Estimated)

August 2, 2026

Study Completion (Estimated)

September 2, 2026

Last Updated

April 21, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

all collected IPD

Available IPD Datasets

Study Protocol Access