The Effect of Transtheoretical Model-based Motivational Interview on Self-efficacy and Illness Compliance

November 22, 2024 updated by: HÜSEYİN ÇAPUK

Aim: This study was planned to determine the effect of transtheoretical model-based motivational interviewing on patients' self-efficacy and disease adherence in patients receiving haemodialysis treatment.

Study design and methods: This study was conducted between June 2022 and April 2023 according to the experimental research model with pre-test and post-test control group. The research was completed with a total of 60 hemodialysis patients, 30 in the experimental group and 30 in the control group.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Turkey
    • Centre
      • Malatya, Centre, Turkey, 44000
        • Inonu University
      • Malatya, Centre, Turkey, 73000
        • Inonu University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

Being on hemodialysis treatment Being able to read and writeH

Exclusion Criteria:

Not knowing how to read or write, Having a psychological disorder that prevents speaking

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: motivational interview group
This group received motivational interviewing training based on the transtheoretical model.
Behavioral: Transtheoretical Model Based Motivational Interviewing
Transtheoretical Model Based Motivational Interviewing was applied to haemodialysis patients in 6 sessions.
Other: routine clinical care
routine clinical care
Experimental: control group
No intervention was performed. Patients continued their routine treatment.
Other: routine clinical care
routine clinical care

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Results
Time Frame: Time Frame: six weeks
A transtheoretical model-based motivational interview was applied to hemodialysis patients in the experimental group.
Time Frame: six weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

HÜSEYİN ÇAPUK

Investigators

  • Study Director: Rukuye Aylaz, Prof. Dr., İnönü Üniversitesi

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 30, 2022

Primary Completion (Actual)

September 30, 2022

Study Completion (Actual)

March 30, 2023

Study Registration Dates

First Submitted

September 27, 2024

First Submitted That Met QC Criteria

November 22, 2024

First Posted (Estimated)

November 27, 2024

Study Record Updates

Last Update Posted (Estimated)

November 27, 2024

Last Update Submitted That Met QC Criteria

November 22, 2024

Last Verified

November 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 112

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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