The Effect of Motivational Interviewing Based on the COM-B Model

NCT06509529 | Not Yet Recruiting

• 1 other identifier: Ordu1
• Study Type: interventional
• Target: 68
• Locations: 0 countries
• Sites: N/A

Brief Summary

This research will be conducted to determine the effect of motivational interviewing based on the COM-B model on women's cervical cancer health beliefs and participation in screening.

Conditions

Cervical Cancer

Keywords

Cervical Cancer; Motivational Interviewing; Early Diagnosis and Screening; Health Beliefs; Nursing; COM-B Model

Outcome Measures

Primary Outcomes (2)

• "Cervical Cancer and Pap Smear Test Health Belief Model Scale"

  The scale was developed by Güvenç et al. (2011). Higher scores from the scale indicate increased sensitivity, caring and motivation; It indicates that benefits are perceived as high for benefit perception and obstacles are perceived as high for obstacle perception.

  0th month and 1st month.

• Status of Cervical Cancer Screening

  This form was prepared by the researcher and will evaluate women's status of being screened for cervical cancer.

  0th month and 1st month.

Study Arms (2)

Experimental group

EXPERIMENTAL

Motivational interviews based on the COM-B Model will be given to the women in the experimental group.

Other: Motivational Interviewing Based on the COM-B Model

control group

NO INTERVENTION

They will receive routine cancer screening information provided by the institution.

Interventions

Motivational Interviewing Based on the COM-B Model OTHER

Motivational Interviewing Based on the COM-B Model will be applied to the women in the experimental group.

Experimental group

Eligibility Criteria

• Age: 30 Years - 65 Years
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Registered at Altınordu Central Family Health Center,
• A woman,
• Between 30-65 years of age,
• The one who is married,
• Have not had a Pap Smear test in the last 5 years,
• Has a smart phone
• Has an internet connection,
• Open to communication and collaboration,
• Women who volunteer to participate in the study will be included in the study.

You may not qualify if:

• Who had total hysterectomy surgery,
• The pregnant one,
• Those diagnosed with cervical cancer and
• Women with a psychiatric diagnosis will be excluded from the study.

Sponsors & Collaborators

• Ordu University: lead

MeSH Terms

Conditions

Uterine Cervical Neoplasms; Disease

Condition Hierarchy (Ancestors)

Uterine Neoplasms; Genital Neoplasms, Female; Urogenital Neoplasms; Neoplasms by Site; Neoplasms; Uterine Cervical Diseases; Uterine Diseases; Genital Diseases, Female; Female Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Urogenital Diseases; Genital Diseases; Pathologic Processes; Pathological Conditions, Signs and Symptoms

Study Officials

• Hacer GÖK UĞUR, Assoc.Prof.

  Ordu University

  STUDY DIRECTOR

Central Study Contacts

Hacer GÖK UĞUR, Assoc.Prof.

CONTACT

04522265200; hacer32@gmail.com

Züleyha Çakır, Nurse

CONTACT

04522265200; cakirzuleyha.379@gmail.com

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Who Masked: PARTICIPANT, OUTCOMES ASSESSOR
• Purpose: OTHER
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Associate Professor.

Study Record Dates

• First Submitted: July 14, 2024
• First Posted: July 19, 2024
• Study Start: August 15, 2024
• Primary Completion: December 30, 2024
• Study Completion: January 30, 2025
• Last Updated: July 19, 2024

Record last verified: 2024-07

Data Sharing

• IPD Sharing: Will not share