Effect of Telenursing on Oral Health
Recruiting · NCT07462221 · Interventional (participants receive a specific treatment) · Lead sponsor: Çanakkale Onsekiz Mart University
View the official record on ClinicalTrials.gov →Interventions studied
reminderstelenursing
What this trial is about
This research will be conducted using a pre-test and post-test control group experimental design to evaluate the effect of telenursing intervention on oral health in individuals with COPD.
Who can take part
Age range
40 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Participants must have been diagnosed with COPD for at least 6 months,
- receive inpatient treatment in internal medicine and surgical clinics,
- signed the informed consent form to participate in the study,
- have internet access and a mobile device with Android/iOS operating system,
- be able to use a phone,
- ≥ 40 years old,
- have no communication barriers,
- mild (Stage 1), moderate (Stage 2), severe (Stage 3), or very severe (Stage 4) stages according to the GOLD (2023) report.
Exclusion criteria
- Those diagnosed with COPD less than 6 months ago,
- Those receiving outpatient treatment,
- Those hospitalized in the intensive care unit,
- Those without internet access and a mobile device with Android/iOS operating system,
- Those who do not have the ability to use a phone,
- Those under 40 years of age,
- Those with communication barriers,
- Those who wish to withdraw from the research/withdraw from participation during the research process,
Where it is running
1 location listed.
- Department of Nursing, Faculty of Health Sciences, Canakkale Onsekiz Mart University - Çanakkale, Turkey (Türkiye)