Online Program to Reduce Depression in MS

NCT02740361 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 279

Last updated 2025-05-20

No results posted yet for this study

Summary

This is an international, multicenter, randomized controlled trial of an internet-based CBT intervention for depression (Deprexis) conducted in five MS centers in the US and Germany. The trial consists of a three-arm primary trial phase and an extension phase targeted at maintenance.

Conditions

Interventions

BEHAVIORAL

Deprexis, DeprexisPlus

Online program Deprexis, either as a stand-alone internet-based intervention (Deprexis) or with added standardized email support by a clinical psychologist (DeprexisPlus). In this trial, we will use a Version of Deprexis that has been adapted to MS-specific needs.

Sponsors & Collaborators

  • National Multiple Sclerosis Society

    collaborator OTHER
  • Universitätsklinikum Hamburg-Eppendorf

    collaborator OTHER
  • Cedars-Sinai Medical Center

    collaborator OTHER
  • University of Missouri, Kansas City

    collaborator OTHER
  • Penn State University

    collaborator OTHER
  • King's College London

    collaborator OTHER
  • University Medical Center Goettingen

    collaborator OTHER
  • NeuroCure Clinical Research Center, Charite, Berlin

    collaborator OTHER
  • Charite University, Berlin, Germany

    lead OTHER

Principal Investigators

  • Stefan M Gold, PhD · Charité University, Berlin

  • Friedemann Paul, MD · Charité University, Berlin

  • Christoph Heesen, MD · Universitätsklinikum Hamburg-Eppendorf

  • Nancy Sicotte, MD · Cedars-Sinai Medical Center

  • Jared Bruce, PhD · University of Missouri, Kansas City

  • Sharon Lynch, MD · University of Missouri, Kansas City

  • Peter Arnett, PhD · Penn State University

  • Rona Moss-Morris, PhD · King's College London

  • Tim Friede, PhD · University Medical Center Goettingen

  • Björn Meyer, PhD · GAIA Group

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-02-15
Primary Completion
2021-01-30
Completion
2021-05-01

Countries

  • United States
  • Germany

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02740361 on ClinicalTrials.gov