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临床试验/NCT05824910
NCT05824910已完成不适用

Effect of Pulmonary Telerehabilitation and Telemonitoring for Patients With Chronic Respiratory Diseases: a Feasibility Study

University of Manitoba2 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2024年5月20日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
16
试验地点
2
主要终点
Change in Dyspnea

研究概览

简要总结

This research study is being conducted to evaluate the feasibility of using technology to deliver a remote home exercise program and assess the health outcomes of patients with chronic lung diseases. Specific objectives are to assess the interventions on patients: 1) Lung function, 2) Dyspnea, 3) Fatigue, 4) Exercise capacity, 5) Self-efficacy, and 6) Health-related quality of life. The investigators will also be evaluating the practicality of using videoconferencing and commercial wearable telemonitoring devices (ie. smart watches) for the implementation of the intervention in this group of patients.

详细描述

This feasibility study uses a one group pre-post intervention study. In a subsequent stage, the possibility of conducting a matched (age, gender, diagnosis) case-control study comparing the effects of this study with the current Pulmonary Rehab WRHA program on patients' outcomes will be explored.

Participants who meet the inclusion criteria will be invited to an initial assessment session of approximately 1 hour (week 0) at the RespirabilityLab (Riverview Health Centre - 4th floor of the Princess Elizabeth Building). A registered therapist in charge of implementing the intervention will request informed consent to participate in the study, explain specifics of the intervention to each participant, and will conduct an initial assessment. Using the participants' initial assessment and personal characteristics, the therapists will provide personalized recommendations (e.g. maximum heart rate, minimum SpO2), and instruct patients on safety precautions (how to pace themselves, when to seek professional or emergency care).

All will receive training in 1) basic device management (join a Zoom meeting, and apps needed), 2) use of a portable spirometer, pulse oximeter and smartwatch, and their associated apps.

Two groups of 6 patients will complete an 8-week program (2 rounds of 12 participants for a total of 24 participants in total). The exercise program will involve a small group of peers (2 groups/6 participants each) in a Zoom meeting 2 times a week/45 min each (including 5 min before and 10 min after the meeting for free talk-chat between the participants e.g. questions, perceptions, etc.). The RA will organize the Zoom meetings, will resolve general questions (e.g. equipment, platforms, etc.) and will act as a direct point of contact between the therapist and the participants. An education session (~30-45 min) will be offered to all participants (12 at a given time) once a week over the 8 weeks on key topics such as managing smoking cessation, managing shortness of breath, exercising with chronic lung disease, managing fatigue, etc. Patients will be asked to always wear a smartwatch and a pulse oximeter while exercising so that they can control their pace while avoiding exceeding target values (HR, Sp02). After each exercise session, participants will be asked to open apps on their smartphone or tablet linked to the wearable devices via Bluetooth so that the data can be transmitted to the research team (Labfront dashboard) or emailed to the RA (CVS format). Participants will be able to contact the therapist or the RA at any time during the study if they have questions or concerns. Otherwise, the patients will be contacted if abnormal values are identified in the telemonitoring data.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • confirmed diagnosis of COPD or ILD
  • living in Manitoba
  • Access to smart phone or tablet and home internet service

排除标准

  • acute exacerbation of their condition
  • history of neurological disease or mental illness
  • inability to ambulate independently without supervision
  • inability to complete basic tasks on a smart phone or tablet

结局指标

主要结局

Change in Dyspnea

时间窗: 8 weeks

Modified Borg Scale (0 "best" to 10 "worse") will be used to assess dyspnea.

Change in Lung Function

时间窗: 8 weeks

% predicted FEV1 and FVC will be assessed using a SpiroBank Smart F/V multi parameter spirometer (MIR) at pre-post intervention and once a week in between to monitor changes. This portable spirometer, which is MDSAP approved and complaint with ATS/ ERS guidelines, connects automatically via Bluetooth to an iOS \& Android compatible App (MIR Spirobank).

Change in Self-efficacy

时间窗: 8 weeks

Assessed using the Self-Efficacy for Managing Chronic Disease 6-Item Scale each rated from 0 "not at all confident" to 10 "totally confident")

Change in Dyspnea severity

时间窗: 8 weeks

Assessed with the modified Medical Research Council (0-4 "higher is worse outcome").

Change in Fatigue

时间窗: 8 weeks

Fatigue severity scale (0 -7 "higher worse") will be used to measure the severity of fatigue.

Change in Exercise Capacity

时间窗: 8 weeks

Assessed with the one-minute sit-to-stand test (number of times the persons can complete the task in one minute).

Change in Health Relate quality of life

时间窗: 8 weeks

Assessed with the Clinical COPD Questionnaire (Scored from 0 - 6 \[worse\])

Impact of cough on quality of life

时间窗: 8 weeks

Assessed with the Leicester Cough Questionnaire (3 - 21 points). Lower scores indicate higher impact of cough on quality of life

Level of Dysphagia

时间窗: 8 weeks

Assessed with the Sydney Swallow Questionnaire(0-100mm "higher represent worse outcome").

次要结局

  • Participant feedback questionnaire(8 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Diana C Sanchez-Ramirez, PhD

Assistant Professor

University of Manitoba

研究点 (2)

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