Discovering Factors in the Clinical Study Journey of Patients With OCD

Description

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

Study Overview

Study Details

Study overview

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.

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

Discovering Factors in the Clinical Study Journey of Patients With OCD

Condition
OCD
Intervention / Treatment

-

Contacts and Locations

San Francisco

Power Life Sciences, San Francisco, California, United States, 94107

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility 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.
  • * 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

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Power Life Sciences Inc.,

Michael B Gill, STUDY_DIRECTOR, Power Life Sciences Inc.

Study Record Dates

2026-06