Study to Verify the Feasibility of Collecting a Broad Variety of Individual Health Data
NCT ID: NCT03135678
Last Updated: 2017-05-31
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.
COMPLETED
12 participants
OBSERVATIONAL
2017-05-12
2017-05-23
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Feasibility of collecting individual health data within the OBSERVE PILOT is described as the ease of gathering a broad variety of data by assessing: (1) the willingness of the subjects to participate in the study, (2) the logistics corresponding with the variety, and (3) the regulatory aspects of gathering a broad variety of data.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Extensive Prospective Validation Study of the NightOwl Home Sleep Apnea Test
NCT03635918
Prospective Validation Study of a Novel Type IV Home Sleep Apnea Test
NCT03385187
Investigating the Physiology of Labour and Labour Onset Through Longitudinal Measurements Performed With a Wearable Sensor
NCT03982654
Non-Contact Monitoring of Subjects With an Optical Device: A Pilot Usability Study
NCT04182165
Gait Analysis Parameter and Upper Limb Evaluation in Control Participants
NCT07136506
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
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* The subject must be older than 18 years old.
Exclusion Criteria
* The subject should not be allergic to eye drops.
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Hilbert Paradox NV
INDUSTRY
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Stefan Verheye, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Director at Hilbert Paradox
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
General Practice
Antwerp, , Belgium
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
OBS_001
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.