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Consequences of Respiratory Devices on Caregivers (CAP2)

NCT04632836 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 350

Last updated 2022-07-27

No results posted yet for this study

Summary

The promoter of the study will conduct a monocentric cohort study that aim to evaluate the consequences of home respiratory devices on patient caregivers' quality of life.

The investigators will examine the impact of home respiratory devices on quality of life in general, sleep quality, anxiety and humour depending on equipment type (Non-invasive ventilation (NIV), continuous positive airway pressure (CPAP) or long-term oxygen therapy (LTOT)) for patients and partners. The investigators will assess the correlation between patient and caregiver's answers. The investigators will assess the correlation between couple's quality of life and adherence to treatment.

To do this, the investigators will use four quality of life questionnaires and the investigators will collect demographic data, medical data and usage report from the equipment.

Conditions

  • Quality of Life

Interventions

OTHER

quality of life questionnaires

responses for quality of life questionnaires (WHOQOL-BREF questionnaire, study specific questionnaire, PSQI index, HADS scale)

Sponsors & Collaborators

  • Asten Sante

    lead INDUSTRY

Principal Investigators

  • Maxime Patout · APHP-Sorbonne Université, Service des Pathologies du Sommeil (Département R3S) Paris, France

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-01-20
Primary Completion
2023-05-01
Completion
2023-05-01

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04632836 on ClinicalTrials.gov