Recruiting NCT04236726
Investigating Health Related Quality of Life in Patients With Chronic Respiratory Failure
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Questionnaire.
- Who it may be relevant to
- Registry conditions: Chronic Obstructive Pulmonary Disease, Respiratory Failure, Neuromuscular Diseases, Ventilatory Failure. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United Kingdom
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
To determine the quality of life of patients living with chronic respiratory failure and the impact interventions have on it.
Detailed description
To determine the quality of life of patients living with chronic respiratory failure and the impact interventions have on it.
Interventions
- Other Questionnaire
HRQoL questionnaires
Primary outcome measures
- HRQoL score [Time frame: Day 0: At the first outpatient clinical consultation with the clinical team]
Secondary outcome measures (1)
- Change in HRQoL score [Time frame: 6 months following first assessment for Outcome 1]
Eligibility criteria
Inclusion criteria
Diagnosed with chronic respiratory failure receiving any of:
- Non-invasive ventilation
- Prolonged mechanical ventilation
- Mechanical insufflation-exsufflation therapy
Exclusion criteria
- Aged <18
- Significant physical or psychiatric co-morbidity that would prevent compliance with trial protocol
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
United Kingdom · 1 center
- Guy's and St. Thomas NHS Foundation Trust — London
Identifiers
NCT: NCT04236726 · CRF-QoL