Discovering Factors in the Clinical Study Journey of Patients With OCD
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorPower Life Sciences Inc.
About this trial
This research aims to collect comprehensive data on the clinical trial experience of OCD patients. Its goal is to identify the factors that limit patients' ability to join or complete a trial successfully. Clinical trial participation often favors specific demographic groups, and limited research exists on the impact of trial attributes on participation. Therefore, this study aims to analyze data from various demographic groups and identify any recurring trends that could provide valuable insights for future OCD patients.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed.
Participant has a diagnosis of OCD.
Willing and able to comply with scheduled visits, treatment schedule, laboratory tests and other requirements of the study.
Disqualifiers
Pregnant or lactating woman
Enrolled in another research study
Any mental or medical condition that prevents the patient from giving informed consent or participating in the trial
Trial population
Participants with OCD who are actively considering involvement in an observational clinical trial, but have not yet completed enrollment and registration.
Trial design
Design model
Case-crossover
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
No trial groups listed
Trial outcomes
Primary outcomes
1
Rate of participants who decide to enroll in a OCD clinical study.
Time frame
3 months2
Number of OCD patients who remain in clinical trial until completion.
Time frame
12 monthsSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov