Obsessive-Compulsive Disorder, OCD
Conditions
Keywords
OCD, Obsessive-Compulsive Disorder
Brief summary
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.
Interventions
None listed
Sponsors
Power Life Sciences Inc.
Study design
Observational model
CASE_CROSSOVER
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* 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.
Exclusion criteria
* 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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rate of participants who decide to enroll in a OCD clinical study. | 3 months |
| Number of OCD patients who remain in clinical trial until completion. | 12 months |
Countries
United States
Contacts
Primary ContactMichael B Gill
Outcome results
None listed