- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02453438
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
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
-
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Massachusetts
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Boston, Massachusetts, United States, 02134
- Massachusetts General Hospital Bipolar Clinic and Research Program
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-
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
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.