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Recruiting NCT06733662

The Effect of Motivational Interviewing-Based Education on Treatment Adherence and Self-Care Agency in COPD Patients

No phase Interventional Motivational Interviewing COPD

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Experimental: Education-based motivational interviewing Group.
Who it may be relevant to
Registry conditions: Motivational Interviewing, COPD. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

The Effect of Motivational Interviewing-Based Education on Treatment Adherence and Self-Care Agency in COPD Patients: A Randomized Controlled Trial

Overview

This randomized controlled trial will be conducted to evaluate the effect of education and motivational interviewing on treatment adherence and self-care power in COPD patients. Hypotheses of the Study; H1: Education and motivational interviewing in COPD patients increase treatment adherence in patients. H2: Education and motivational interviewing in COPD patients increase self-care power in patients. There will be two groups in the study: control and intervention groups. Before the intervention, pre-test data will be collected in the control and intervention groups. After the intervention, post-test data will be collected in both groups in line with the data collection forms.

Detailed description

In line with the randomization list, patients will be assigned to the intervention and control groups in line with the inclusion criteria. Pre-test data will be collected face-to-face in the intervention group in accordance with the data collection forms. After collecting the pre-test data, the patient will be allowed to rest for about 10 minutes, and then COPD training will be given to the patient in a single session lasting about 45-50 minutes in line with the training booklet and by evaluating the pre-test data. The education booklet will be given to the patient. On the 3rd day, the first session of motivational interview will be held. On the 5th day and 7th day and 15th day, motivational interview sessions will continue with the patients. During the motivational interview, patients will be supported in line with the training booklet. On the 30th day, the patient will be interviewed face-to-face and post-test data will be collected.

Patients in the control group will be interviewed and no intervention will be made after the pre-tests are applied. Patients in the control group will continue their routine controls. In the final test (1st month), an appointment date will be set with the patient and the final test data will be collected face-to-face.

Interventions

  • Behavioral Experimental: Education-based motivational interviewing Group
    The Effect of Motivational Interviewing-Based Education on Treatment Adherence and Self-Care Agency in COPD Patients

Primary outcome measures

  • Morisky 8-item Medication Adherence Scale [Time frame: 0 days]
  • Morisky 8-item Medication Adherence Scale [Time frame: 30 days]
  • Self-care Agency Scale [Time frame: 0 days]
  • Self-care Agency Scale [Time frame: 30 days]

Eligibility criteria

Inclusion criteria

  • Confirmed diagnosis of COPD for at least 6 months
  • Admitted to the chest clinic
  • No communication problems
  • Patients who volunteered to participate in the study.

Exclusion criteria

  • In the period of exacerbation
  • Uncooperative due to dyspnea
  • With a malignant disease
  • Patients with a confirmed diagnosis of psychiatric illness

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Supportive care

Study locations

Turkey (Türkiye) · 1 center
  • Kahramanmaraş Istiklal Universty — Kahramanmaraş

Identifiers

NCT: NCT06733662 · IstiklalU-YSazak-003

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗