The Effect of Telenursing Interventions in Empowering Patients With COPD

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

90 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-06-25

Study Completion Date

2024-11-25

Brief Summary

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The aim of this study is to evaluate the effect of telenursing interventions based on the empowerment model in empowering patients with COPD.

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Detailed Description

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Patient empowerment is gaining importance and popularity day by day as it can be sustained through telehealth applications. The importance of using communication technologies in providing health care services has become more evident during the COVID-19 pandemic. When integrated into healthcare, technology-centric services provide continuous and easily accessible health data for patients and help facilitate self-monitoring. With tele-nursing, COPD patients can be strengthened in health literacy by teaching them how to access accurate and reliable resources. Through tele-nursing, online support groups and forums can be created among COPD patients so that patients can share their experiences with each other. In this way, social support is provided to patients who have to remain in social isolation due to their illness.

Conditions

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Copd Empowerment Empowerment, Patient Self Efficacy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Two groups with experimental and control groups

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

DOUBLE

Participants Outcome Assessors

In order to prevent selection bias in the study, the assignment to the experimental and control groups will be made on a computer by a person who is unfamiliar with the research process. Individuals included in the study will not be told whether they are in the experimental or control group. The analysis of the data will be done by a statistics expert who is outside the research process.

Study Groups

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Telenursing Interventions Group

Participants in this group will receive five hours of face-to-face empowerment training. After the training, the experimental group will be monitored remotely by the researcher nurse via tele-nursing interventions for 12 weeks. Participants will be given a pulse oximeter, symptom diary, action plan, oxygen saturation-pulse monitoring chart. Participants will be asked to measure their oxygen saturation and pulse once a day for 12 weeks and record it on the chart. Participants will also be asked to record their complaints in their symptom diary. Participants will be called by the researcher every two weeks (on Thursdays) and informative and reminding text messages prepared specifically for the disease will be sent to the participants three times a week for 12 weeks. Participants will be able to reach the researchers by phone whenever they need.

Group Type EXPERIMENTAL

Telenursing Interventions

Intervention Type OTHER

Patient follow-up with phone calls and text messages

No Intervention Group

Participants in this group will be given a pulse oximeter, symptom diary, action plan, oxygen saturation-pulse monitoring chart. No intervention will be taken.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Telenursing Interventions

Patient follow-up with phone calls and text messages

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Having a confirmed COPD diagnosis for at least one year
* being literate,
* Having the cognitive and mental competence to answer questions,
* Being able to use a mobile phone,
* Disease symptoms are at a level that does not interfere with communication,
* Being in COPD Stage 2 and Stage 3 according to the Global Initiative for Chronic Obstructive Lung Disease (GOLD: Global Initiative for Chronic Obstructive Lung Disease) criteria (30% ≤ FEV1 \<80% (of expected)),

Exclusion Criteria

* The disease is in the acute exacerbation period,
* Dyspnea is at a level that prevents cooperation,
* Having sensory loss regarding vision, hearing and speech,
* Refusal to sign informed consent forms
* It is the refusal of the research to complete the data collection tools.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No