跳至主要内容
临床试验/NCT07462221
NCT07462221招募中不适用

The Effect of Telenursing Interventions on Oral Health in Individuals With COPD

Çanakkale Onsekiz Mart University1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2026年3月4日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
80
试验地点
1
主要终点
oral healt

研究概览

简要总结

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.

详细描述

Studies evaluating the effectiveness of oral health interventions in individuals with COPD are limited in the literature. Maintaining oral health is a crucial part of patient care. Sustainable nursing interventions are necessary from the onset of the disease to the end of life. Patient education conducted by nurses is important in improving medication adherence and preventing comorbidities. Furthermore, it is known that practices involving a multidisciplinary team approach with nurse participation reduce readmissions and hospital stays for COPD patients. Therefore, this study aims to evaluate the effect of telenursing intervention on oral health in individuals with COPD. The experimental group will receive oral health education via telenursing intervention (via video call) and daily oral health reminders. The control group will not receive education. Oral health education for the experimental group is planned to be given within 24 hours after the pre-test. The experimental group will be invited to the hospital one month after the oral health education for evaluation of oral health and quality of life related to oral health, and the control group will be invited one month after the pre-test.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
40 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • 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,

研究组 & 干预措施

experimental group

Experimental

The experimental group will receive oral health education via telenursing intervention (via video call) and daily oral health reminders. Oral health education for the experimental group is planned to be given within 24 hours after the pre-test. Participants will also receive reminders regarding oral hygiene, including "performing oral care at least twice a day, every day" and "rinsing their mouths with water after using an inhaler." The experimental group will be invited to the hospital one month after the oral health education for evaluation of oral health and quality of life related to oral health.

干预措施: telenursing (Behavioral)

experimental group

Experimental

The experimental group will receive oral health education via telenursing intervention (via video call) and daily oral health reminders. Oral health education for the experimental group is planned to be given within 24 hours after the pre-test. Participants will also receive reminders regarding oral hygiene, including "performing oral care at least twice a day, every day" and "rinsing their mouths with water after using an inhaler." The experimental group will be invited to the hospital one month after the oral health education for evaluation of oral health and quality of life related to oral health.

干预措施: reminders (Behavioral)

control group

No Intervention

The control group will not receive training. They will be invited to the hospital for an oral health and quality of life check one month after the initial follow-up.

结局指标

主要结局

oral healt

时间窗: pre-test and post-test (1 month)

The Oral Assessment Guide (ADR) will be used to evaluate oral health. The guide supports the creation of an oral care protocol for patients with impaired oral mucosal membranes. Scores on the guide range from 8 to 24. According to the ADR, a low score indicates good oral health, while a high score indicates negative changes in oral health. The oral mucosal membrane score will be evaluated in both pre-test and post-test. A light source and a tongue depressor (one for each participant) are planned to be used during the oral health assessment.

Quality of Life Related to Oral Health

时间窗: pre-test and post-test (1 month)

The scale has seven sub-dimensions: 'Functional Limitation', 'Physical Pain', 'Psychological Distress', 'Physical Disability', 'Psychological Disability', 'Social Disability', and 'Handicap'. Scores obtainable from the Oral Health Impact Scale range from 0 to 56. Since all questions are in a negative form, a score close to 0 indicates good quality of life related to oral and dental health, while a score close to 56 indicates poor quality of life related to oral and dental health. A high score on the scale indicates low quality of life related to oral health.

次要结局

未报告次要终点

研究者

发起方
Çanakkale Onsekiz Mart University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Sevda Ateş

Associate Professor

Çanakkale Onsekiz Mart University

研究点 (1)

Loading locations...

相似试验