The Effect of Post-Discharge Multiple Nursing Interventions on the Number of Hospital Admissions, Dyspnea Level, and Quality of Life in COPD Patients Receiving Home Oxygen Therapy: A Randomized Controlled Study

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Chronic obstructive pulmonary disease (COPD) is a progressive lung disease characterized by persistent airflow obstruction and chronic respiratory symptoms or alpha-1-antitrypsin deficiency in response to inhaled cigarette smoke or other irritants. The excessive morbidity and mortality associated with COPD acute exacerbations represent a significant public health problem that places a high burden on patients, their families and society. In frequent and severe exacerbations, patients may experience a decrease in quality of life, depression, and even death up to one year after hospitalization. Costs associated with COPD are more than $15.5 billion, and hospitalizations and repeated hospital admissions related to acute exacerbations alone account for 70% of all costs. For these reasons, efforts to reduce hospital admissions and hospitalizations associated with recurrent exacerbations are imperative to improve patient's quality of life and reduce the societal burden.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Being diagnosed with stage 4 (group D) COPD according to GOLD criteria

• Being 18 years or older,

• Having a video computer, tablet or phone,

• Having an internet connection at home or on the phone,

• Residing in the city centre of Konya,

• Not having a communication problem, such as an inability to understand/speak Turkish, that would prevent participation in the research,

• Being literate,

• Using an oxygen concentrator at home.

Locations
Other Locations
Turkey
Selçuk Tıp Fakültesi Hastanesi
RECRUITING
Konya
Contact Information
Primary
HASAN BAKIR
smhasanbakir@gmail.com
05055346870
Time Frame
Start Date: 2023-02-15
Estimated Completion Date: 2024-12-31
Participants
Target number of participants: 74
Treatments
Experimental: intervention group
Within the scope of the pre-test, the researcher to the patients who will explain the purpose of the research and agree to participate in the research; Inclusion Criteria Form; Socio-Demographic Information Form; Patient Descriptive Information Form, Modified British Medical Research Council (MRC) Questionnaire, St George Respiratory Questionnaire (Quality of Life Scale) will be used to evaluate patients' symptoms. In addition, the patients in the intervention group will be educated with the training booklet Educational Guide for COPD Patients prepared by the researcher by scanning the literature.
No_intervention: Not intervention group
The control group will be subjected to the standard COPD training given in the hospital and no intervention will be made by the researcher. After the trials of the experimental group are completed, the control group will be given a home visit, a COPD training booklet, and audio-visual materials.
Sponsors
Leads: Necmettin Erbakan University

This content was sourced from clinicaltrials.gov