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RECRUITINGOBSERVATIONAL

Discovering Factors in the Clinical Study Journey of Patients With OCD

Understanding the Patient Perspective: An Observational Study on Experiences of OCD Clinical Trial Patients

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

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.

Who May Be Eligible (Plain English)

Who May Qualify: - Ability to provide written willing to sign a consent form 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. Who Should NOT Join This Trial: - Pregnant or lactating woman - Enrolled in another research study - Any mental or medical condition that prevents the patient from giving willing to sign a consent form or participating in the trial Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
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

Locations (1)

Power Life Sciences
San Francisco, California, United States