The Impact of Training on Self-Efficacy, Symptom Level, and Activities of Daily Living

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorIstanbul Saglik Bilimleri University

About this trial

This study is a randomized, controlled experimental trial with a pretest-posttest design, conducted to evaluate the effects of Pecha Kucha-based education on self-efficacy, symptom level, and activities of daily living in individuals diagnosed with chronic obstructive pulmonary disease (COPD) receiving noninvasive mechanical ventilation support.

The study will include two groups, and intergroup differences will be evaluated:

1. Control group 2. Intervention group

Study Hypotheses H1: Pecha Kucha-based education on noninvasive mechanical ventilation (NIMV) support provided to individuals with chronic obstructive pulmonary disease (COPD) increases patients' self-efficacy levels.

H2: Pecha Kucha-based education on noninvasive mechanical ventilation (NIMV) support provided to individuals with chronic obstructive pulmonary disease (COPD) reduces patients' symptom levels.

H3: Pecha Kucha-based education on noninvasive mechanical ventilation (NIMV) support provided to individuals with chronic obstructive pulmonary disease (COPD) improves patients' activities of daily living.

Eligibility criteria

Qualifiers

Age 18 years or older

Diagnosed with chronic obstructive pulmonary disease (COPD) at least one year prior

Currently receiving treatment with noninvasive mechanical ventilation (NIMV) support

Ability to communicate verbally and in writing in a clear and sustainable manner

Disqualifiers

Failure to attend planned educational sessions or inability to complete the study protocol

Voluntary withdrawal from the study, declared verbally or in writing

Death during the study period

Development of a serious health condition preventing continuation in the education program (e.g., hospitalization, acute exacerbation, deterioration in mental status)

Trial design

Treatments tested in this trial

  • Intervention Group

Treatment groups

60 Participants
are divided into 2 treatment groups

Locations

This trial has no locations