Mood Patient Powered Research Network (MoodNetwork)

September 5, 2019 updated by: Andrew A. Nierenberg, MD, Massachusetts General Hospital
The MoodNetwork, a patient-powered research network (PPRN), is one of 18 PPRNs participating in Patient-Centered Outcomes Research Institute's (PCORI) PCORnet network. Its objective is to improve the nation's capacity to conduct comparative effectiveness research that reflects questions of greatest importance to patients and other stakeholders. A robust data infrastructure will be built that, in phase one, allows participants to contribute data, including those from participant questionnaires, visualize their own health information in intuitive and helpful ways, and share their aggregated de-identified health information within and outside of the Network.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

5716

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • Massachusetts
      • Boston, Massachusetts, United States, 02134
        • Massachusetts General Hospital Bipolar Clinic and Research Program

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.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

English speaking individuals over 18 years of age who self-identify as having a mood disorder.

Description

Inclusion Criteria:

  • English speaking
  • Valid email address
  • Self-identify as having a mood disorder

Exclusion Criteria:

  • Under 18 years of age

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Patient Reported Outcomes Working Group Items Questionnaire
Time Frame: average of 3 years
average of 3 years
Composite International Diagnostic Interview Mania Questionnaire
Time Frame: average of 3 years
average of 3 years
Mini International Neuropsychiatric Interview Depression
Time Frame: average of 3 years
average of 3 years
Quick Inventory of Depressive Symptoms Self Report
Time Frame: average of 3 years
average of 3 years
Altman Self Rated Mania Scale
Time Frame: average of 3 years
average of 3 years
WHO-five well-being index (WHO-5)
Time Frame: average of 3 years
average of 3 years
Depression and Bipolar Support Alliance Wellness Tracker Questionnaire
Time Frame: average of 3 years
average of 3 years
Experience of Care and Health Outcomes Questionnaire
Time Frame: average of 3 years
average of 3 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Massachusetts General Hospital

Investigators

  • Principal Investigator: Andrew A Nierenberg, M.D., Massachusetts General Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 1, 2015

Primary Completion (Actual)

March 1, 2019

Study Completion (Actual)

March 1, 2019

Study Registration Dates

First Submitted

May 5, 2015

First Submitted That Met QC Criteria

May 22, 2015

First Posted (Estimate)

May 25, 2015

Study Record Updates

Last Update Posted (Actual)

September 6, 2019

Last Update Submitted That Met QC Criteria

September 5, 2019

Last Verified

September 1, 2019

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2014P001346

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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