Discovering Factors in the Clinical Study Journey of Patients With OCD

Purpose

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.

Conditions

  • OCD
  • Obsessive-Compulsive Disorder

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts 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

Study Design

Phase
Study Type
Observational
Observational Model
Case-Crossover
Time Perspective
Prospective

Recruiting Locations

More Details

Status
Recruiting
Sponsor
Power Life Sciences Inc.

Study Contact

Michael B Gill
415-900-4227
bask@withpower.com