Development of a Targeted Patient Portal Intervention to Improve Depression Treatment Adherence and Outcomes

NCT ID: NCT04646681

Last Updated: 2022-06-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-03-31

Study Completion Date

2022-04-30

Brief Summary

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

Detailed Description

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This study is being done in 3 phases. First 2 phases were observational with total enrollment of 300 subjects. The final 3rd phase is interventional and we are anticipating to enroll 50 subjects. It is described below.

Patients being treated for depressive symptoms at the University of Iowa, Department of Psychiatry are invited to participate. Participants will complete a remote (phone or video) visit. After being informed about the study and potential risks, those who consent to being in the study will be assigned to one of two groups. They will complete an online survey and receive some basic training on patient portals. After the visit. both groups will be followed for 6 months. Depending on their group assignment, they will complete:

* two to five phone calls with a study team member and
* two to five online questionnaires

Conditions

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Depression

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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Group 1

Group Type EXPERIMENTAL

ConnectCare

Intervention Type BEHAVIORAL

increased monitoring between clinical mental health visits

Group 2

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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ConnectCare

increased monitoring between clinical mental health visits

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* English speaking,
* PHQ-9 score of 10 or higher (questions 1-8 only),
* Taking medication for depressive symptoms,
* 1 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

Exclusion Criteria

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

18 Years

Maximum Eligible Age

89 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Carolyn L Turvey

OTHER

Sponsor Role lead

Responsible Party

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Carolyn L Turvey

Professor

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Carolyn Turvey, phD

Role: PRINCIPAL_INVESTIGATOR

University of Iowa

Locations

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

Iowa City, Iowa, United States

Site Status

Countries

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United States

Other Identifiers

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201805861

Identifier Type: -

Identifier Source: org_study_id

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