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OpenTrials
Completed

NCT Number: NCT02453438

Mood Patient Powered Research Network (MoodNetwork)

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Massachusetts General Hospital Bipolar Clinic and Research Program

Boston, Massachusetts, 02134, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • Under 18 years of age

Treatment and study plan

Patient reported outcomes

Other

Patient reported outcomes will be collected using a variety of questionnaires that assess mood symptoms.

Primary outcomes

  1. Patient Reported Outcomes Working Group Items Questionnaire

    Time frame: average of 3 years

  2. Composite International Diagnostic Interview Mania Questionnaire

    Time frame: average of 3 years

  3. Mini International Neuropsychiatric Interview Depression

    Time frame: average of 3 years

  4. Quick Inventory of Depressive Symptoms Self Report

    Time frame: average of 3 years

  5. Altman Self Rated Mania Scale

    Time frame: average of 3 years

  6. WHO-five well-being index (WHO-5)

    Time frame: average of 3 years

  7. Depression and Bipolar Support Alliance Wellness Tracker Questionnaire

    Time frame: average of 3 years

  8. Experience of Care and Health Outcomes Questionnaire

    Time frame: average of 3 years

Sponsors and collaborators

Lead sponsor

Massachusetts General Hospital

Other

Registry information

Important dates

Study start
2015
Primary completion
2019
Study completion
2019
First posted
May 25, 2015
Registry last updated
Sep 6, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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