The Effect of Training Given to Patients With COPD in Line With Pender's Health Promotion Model

Not Applicable

Completed

• Conditions: Chronic Obstructive Pulmonary Disease; Self Efficacy
• Interventions: Behavioral: Intervention group trained in line with the Health Promotion Model

• Registration Number: NCT06551103
• Lead Sponsor: TC Erciyes University

Brief Summary

This study was conducted as a randomized controlled experimental study. The study was conducted with patients hospitalized in the chest diseases intensive care unit of a state hospital. The study was terminated with the participation of 140 patients, 70 in each group. Data were collected with Descriptive Information Form and COPD Self-Efficacy Scale.

Detailed Description

This study was conducted as a randomized controlled experimental study. The study was conducted with patients hospitalized in the chest diseases intensive care unit of a state hospital. The study was terminated with the participation of 140 patients, 70 in each group. Data were collected with the Descriptive Information Form and COPD Self-Efficacy Scale. Self-efficacy of all patients was assessed at the beginning of the study. Patients in the intervention group were given training prepared in line with the health promotion model. The control group received standard practices of the clinic. After three months, patients' self-efficacy was re-evaluated.

Study Timeline

• Study Start: 2023-12-01
• Primary Completion: 2024-06-30
• Study Completion: 2024-06-30
• Status Verified: 2024-08
• Study First Submitted: 2024-08-09
• Study First Submitted QC: 2024-08-09
• Last Update Submitted: 2024-08-09
• Study First Posted: 2024-08-13
• Last Update Posted: 2024-08-13

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 140

Inclusion Criteria

• being 18 years of age or older,
• having been diagnosed with COPD at least 6 months ago,
• volunteering to participate in the study,
• being able to speak and understand Turkish and communicate effectively,
• not having a mental or physical disability that would prevent answering the questions.

Exclusion Criteria

• having a psychiatric illness,
• having vision and hearing problems,
• having cognitive dysfunction,
• not volunteering to participate in the study.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Intervention group trained in line with the Health Promotion Model	Intervention group trained in line with the Health Promotion Model	A literature review was conducted by the researchers within the scope of Health Promotion Model and a educational material was prepared. With this educational material, the patients in the intervention group were trained in four sessions lasting 25 minutes each.

Primary Outcome Measures

Name	Time	Method
Self-Efficacy	3 months after the first test	Self-efficacy was assessed with the COPD Self-Efficacy Scale. The 34-item COPD Self-Efficacy Scale has 5 sub-dimensions. The items in the scale are ranked from very safe (5 points) to not safe at all (1 point) and are Likert-type. In the evaluation of the scale, the higher the score obtained from the scale, the higher the competence level of the individual in managing respiratory difficulty.

Trial Locations

Locations (1)

Sevda Korkut; 🇹🇷 Talas, Kayseri, Turkey