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

NCT ID: NCT06509529

Last Updated: 2024-07-19

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 68 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-08-15
• Study Completion Date: 2025-01-30

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.

Detailed Description

Cancer is an important public health problem in terms of mortality and morbidity in the world and in our country, and ranks second among the causes of death. It can reduce the mortality and morbidity rate in cancer with early diagnosis and screening studies. One of the cancers for which early diagnosis and screening studies are carried out in women is cervical cancer, and it is the 4th most frequently diagnosed cancer type that causes death in women. Although early diagnosis and screening studies are carried out, women do not participate in enough cervical cancer screenings for different reasons. Interventions are needed to increase women's motivation to participate in screening. 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. The research is planned as a parallel group single-blind randomized controlled experimental study and will be conducted on women between the ages of 30-65 who are registered at Altınordu Central Family Health Center in Ordu Province. The population of the research will be women between the ages of 30-65 who are registered at Altınordu Central Family Health Center, and the sample will be 74 women who meet the research criteria and agree to participate in the research. The data of the research will be collected with the "Information Form", "Cervical Cancer and Pap Smear Test Health Belief Model Scale", "Cervical Cancer Screening Status Evaluation Form" and "Satisfaction Evaluation Form". A motivational interview program based on the COM-B Model will be applied to the women in the experimental group for 1 month (1st week face-to-face, 2nd, 3rd and 4th weeks online). No intervention will be applied to the control group during the research process. The analysis of the data will be done in a computer environment by an expert statistician. Necessary institutional permissions and ethics committee approval will be obtained for the research.

Conditions

Cervical Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: DOUBLE

Study Groups

Experimental group

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

Group Type: EXPERIMENTAL

Motivational Interviewing Based on the COM-B Model

Intervention Type: OTHER

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

control group

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

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Motivational Interviewing Based on the COM-B Model

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

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• 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.

Exclusion Criteria

• 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.

• Minimum Eligible Age: 30 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

Ordu University

OTHER

Sponsor Role: lead

Responsible Party

Hacer Gok Ugur

Associate Professor.

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Hacer GÖK UĞUR, Assoc.Prof.

Role: STUDY_DIRECTOR

Ordu University

Central Contacts

Hacer GÖK UĞUR, Assoc.Prof.

Role: CONTACT

hacer32@gmail.com

04522265200

Züleyha Çakır, Nurse

Role: CONTACT

cakirzuleyha.379@gmail.com

04522265200

Other Identifiers

Ordu1

Identifier Type: -

Identifier Source: org_study_id