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Набор скоро начнётся NCT07747571

Factors Associated With Acceptance of Home-Based Pulmonary Telerehabilitation in COPD

Наблюдательное Chronic Obstructive Pulmonary Disease (COPD) Pulmonary Rehabilitation

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: No intervention.
Кому может быть актуально
Состояния в реестре: Chronic Obstructive Pulmonary Disease (COPD), Pulmonary Rehabilitation. Базовые параметры: от 18 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Франция
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Factors Associated With Acceptance or Refusal of Participation in a Home-Based Pulmonary Telerehabilitation Program Among Adults With Chronic Obstructive Pulmonary Disease: A Retrospective Study

Обзор

Pulmonary rehabilitation improves symptoms, exercise capacity, and quality of life in people with chronic obstructive pulmonary disease (COPD), but access and participation may be limited by travel, organizational, logistical, and personal barriers. Home-based pulmonary telerehabilitation may reduce some of these barriers, although not all eligible individuals accept this mode of care. Identifying the characteristics associated with acceptance or refusal of this model is therefore essential to better define the population most likely to benefit from this approach, tailor the program's delivery and content, and identify potential remaining barriers in order to improve access to care. This retrospective study will use existing data from adults with COPD who were screened at ADIR Association between May 2024 and April 2025 for an 8-week home-based pulmonary telerehabilitation feasibility study. Of 50 potentially eligible individuals, 21 accepted participation and 29 declined. Demographic, clinical, functional, psychological, and geographic characteristics will be compared between individuals who accepted and those who declined participation. Documented reasons for refusal will be described, and factors associated with refusal will be explored using logistic regression.

Подробное описание

ACCEPT-TELEREHAB is a single-center retrospective observational cohort study based on data collected during screening for the TELEREHAPP feasibility study (ClinicalTrials.gov identifier NCT05314686). The source cohort comprises all individuals with COPD who were screened and considered potentially eligible for an 8-week home-based pulmonary telerehabilitation program at ADIR Association between May 2024 and April 2025. Participants will be classified according to the decision recorded at screening: acceptance or refusal of the proposed telerehabilitation program.

Data will be extracted from the original screening file, medical records, and information available from the pulmonary rehabilitation referral and assessment. Variables of interest include age, sex, body mass index, COPD severity, comorbidities, available pulmonary function and exercise-test data, long-term oxygen therapy, dyspnea, quality of life, psychological status, functional exercise capacity, previous pulmonary rehabilitation, and the setting of any previous pulmonary rehabilitation program. When a reason for declining participation was documented, it will be coded retrospectively into descriptive categories; more than one category may be assigned to a single participant.

Home-to-center distance and estimated travel time will be derived using a standardized mapping procedure. The residential address available at screening will be used to calculate the fastest car journey to ADIR Association for a standardized arrival time of 9:00 AM on a working Tuesday outside public holidays and school vacations.

Continuous variables will be summarized using means and standard deviations or medians and interquartile ranges, as appropriate. The acceptance and refusal groups will be compared using independent-samples t tests or Wilcoxon-Mann-Whitney tests for continuous variables and chi-square or Fisher exact tests for categorical variables. Differences will be reported with 95 percent confidence intervals. Refusal to participate will be the dependent variable in univariable and multivariable logistic regression models. Results will be reported as odds ratios with 95% confidence intervals.

Вмешательства

  • Другое No intervention
    None for the present retrospective study.

Первичные конечные точки

  • Participation Decision Regarding Home-Based Pulmonary Telerehabilitation [Срок оценки: At screening, before initiation of the proposed 8-week telerehabilitation program]
Вторичные конечные точки (12)
  • Documented Reasons for Refusal of Home-Based Pulmonary Telerehabilitation [Срок оценки: At screening, when the participation decision was documented]
  • Distance From the Participant Residence to the Pulmonary Rehabilitation Center [Срок оценки: At the time of screening]
  • Estimated Travel Time From the Participant Residence to the Pulmonary Rehabilitation Center [Срок оценки: At the time of screening]
  • Age at screening [Срок оценки: At the time of screening]
  • Sex distribution [Срок оценки: At the time of screening]
  • Body mass index at screening [Срок оценки: At the time of screening]
  • Chronic Obstructive Pulmonary Disease Severity [Срок оценки: At the time of screening]
  • Long-term oxygen status [Срок оценки: At the time of screening]
  • Modified Medical Research Council Dyspnea Scale Score [Срок оценки: At the time of screening]
  • Visual Simplified Respiratory Questionnaire Score [Срок оценки: At the time of screening]
  • Saint George's Respiratory Questionnaire [Срок оценки: At the time of screening]
  • Hospital Anxiety and Depression Scale Anxiety Subscale Score [Срок оценки: At the time of screening]

Критерии участия

Критерии включения

  • Adults with COPD who were screened at ADIR Association between May 2024 and April 2025 for an 8-week home-based pulmonary telerehabilitation feasibility study. Please, refer to ClinicalTrials.gov identifier NCT05314686.

Критерии исключения

  • Not applicable

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Когортное

Центры проведения

Франция · 1 центр
  • ADIR Association — Rouen

Идентификаторы

NCT: NCT07747571 · ACCEPT-TELEREHAB

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗