Open/Aftercare Treatment for Participants Diagnosed With Obsessive Compulsive Disorder

NCT ID: NCT03511534

Last Updated: 2025-07-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

200 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-06-23

Study Completion Date

2026-06-30

Brief Summary

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The purpose of this study is to provide participants diagnosed with obsessive compulsive disorder (OCD) and completed one of the active study protocols at the Rodriguez Lab, with open/aftercare treatment.

Detailed Description

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After completing one of the active clinical studies participants have the option to enroll in this protocol that offers open treatment.

The goal is to compare two forms of current standard treatments, psychotherapy vs pharmacotherapy.

Conditions

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OCD

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Participants will choose to enter the psychotherapy or pharmacotherapy arm.
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Psychotherapy

Participants will receive evidenced based psychotherapy by a trained psychologist

Group Type ACTIVE_COMPARATOR

Psychotherapy

Intervention Type BEHAVIORAL

Evidenced based psychotherapy by a trained psychologist

Pharmacotherapy

Participants will receive pharmacotherapy by a psychiatrist

Group Type ACTIVE_COMPARATOR

Pharmacotherapy

Intervention Type OTHER

Pharmacotherapy by a psychiatrist

Interventions

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Psychotherapy

Evidenced based psychotherapy by a trained psychologist

Intervention Type BEHAVIORAL

Pharmacotherapy

Pharmacotherapy by a psychiatrist

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

1. Ability to speak and understand English
2. Capacity to consent (e.g. as determined by assessing the patient's understanding of the risks, benefits, and procedures of the study)
3. Completed an active study protocol at the Rodriguez Lab at Stanford University

Exclusion Criteria

1. Children younger than 18
2. Active suicidality
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Stanford University

OTHER

Sponsor Role lead

Responsible Party

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Carolyn Rodriguez

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Carolyn Rodriguez, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Assistant Professor, Stanford University

Locations

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Stanford University

Stanford, California, United States

Site Status

Countries

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United States

Other Identifiers

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41165

Identifier Type: -

Identifier Source: org_study_id

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