Validating the Use of Frailty Measurements to Predict Care & Quality of Life
NCT ID: NCT06325241
Last Updated: 2024-04-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
ACTIVE_NOT_RECRUITING
123 participants
OBSERVATIONAL
2022-12-12
2025-03-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
This work will provide a foundation in the development of customized interventions for people with COPD and varying degrees of frailty, with the goal of improving quality of life and optimizing health system service delivery for patients and their care givers.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
COPD Care Model on Clinical and Patient-Reported Outcomes
NCT03332394
The Effect of Frailty on Balance, Activities of Daily, and Exercise Capacity in COPD
NCT03840941
Functional Status in COPD Patients After Exercise Rehabilitation Program
NCT06142266
Asymptomatic Versus Symptomatic Mild COPD: Comparisons at Rest and at Exercise
NCT02235025
Research of Endobronchial Optical Coherence Tomography in Pre-COPD
NCT06436482
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
No intervention
There is no intervention. This is an observational study.
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Chronic Obstructive Pulmonary Disease diagnosis confirmed by pulmonary function testing.
* English or French speaking
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ottawa Hospital Research Institute
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Sunita Mulpuru
Staff Physician, Investigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
The Ottawa Hospital, General Campus
Ottawa, Ontario, Canada
Countries
Review the countries where the study has at least one active or historical site.
Provided Documents
Download supplemental materials such as informed consent forms, study protocols, or participant manuals.
Document Type: Study Protocol and Statistical Analysis Plan
Document Type: Informed Consent Form: Verbal consent
Document Type: Informed Consent Form: English Information Sheet
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
20200048-01H
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.