NCT04646681

Brief Summary

The purpose of this research study is to learn how best to use patient portals to help improve the treatment of mood disorders.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable depression

Timeline
Completed

Started Mar 2021

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 20, 2020

Completed
10 days until next milestone

First Posted

Study publicly available on registry

November 30, 2020

Completed
4 months until next milestone

Study Start

First participant enrolled

March 31, 2021

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2022

Completed
Last Updated

June 10, 2022

Status Verified

June 1, 2022

Enrollment Period

1.1 years

First QC Date

November 20, 2020

Last Update Submit

June 9, 2022

Conditions

Depression

Keywords

patient portalstreatment adherence

Outcome Measures

Primary Outcomes (1)

  • Patient Health Questionnaire (PHQ-9)

    measures the severity of depression symptoms

    Once per month for 6 months

Study Arms (2)

Group 1

EXPERIMENTAL
Behavioral: ConnectCare

Group 2

NO INTERVENTION

Interventions

ConnectCareBEHAVIORAL

increased monitoring between clinical mental health visits

Group 1

Eligibility Criteria

Age18 Years - 89 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • English speaking,
  • PHQ-9 score of 10 or higher (questions 1-8 only),
  • Taking medication for depressive symptoms,
  • or more appointments scheduled or planned with University of Iowa psychiatry provider in next 6 months,
  • Home computer w/internet access,
  • MyChart (University of Iowa Healthcare's patient portal) account/MyChart enrollment

You may not qualify if:

  • Psychotic disorder/symptoms,
  • Current substance use disorders (other than alcohol, tobacco, marijuana),
  • Active suicidal ideation within past 1 year,
  • Cognitive impairment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Iowa Carver College of Medicine, Dept. of Psychiatry

Iowa City, Iowa, 52242, United States

Location

MeSH Terms

Conditions

DepressionTreatment Adherence and Compliance

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehaviorHealth Behavior

Study Officials

  • Carolyn Turvey, phD

    University of Iowa

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

November 20, 2020

First Posted

November 30, 2020

Study Start

March 31, 2021

Primary Completion

April 30, 2022

Study Completion

April 30, 2022

Last Updated

June 10, 2022

Record last verified: 2022-06

Data Sharing

IPD Sharing
Will not share

Locations

US(1)