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Improving Depression Via E-Health Access (IDEA) Study

Improving Depression Via E-Health Access (IDEA) Study: Evaluating Uptake and Efficacy of Self-Help e-Mental Health Interventions in Primary Care

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04689568
Enrollment
32
Registered
2020-12-30
Start date
2021-01-27
Completion date
2022-07-01
Last updated
2023-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression

Brief summary

The researchers are doing this study to learn more about which online self-help resources, including a smartphone app, an online program, or an informational website, primary care patients with depression are likely to choose and whether the chosen tool will improve their depressive symptoms and wellbeing. The researchers would also like to know how likely someone is to use the resources and their satisfaction with the resources.

Detailed description

Participants will be using a self-help resource for the 6-week study period. A Care Manager will contact participants by phone, once a week, for about 5-10 minutes at a pre-arranged time. Participation will be needed for 10 weeks in total (6 weeks of active participation and a survey 1-month after the study intervention ends). Subscription-based self-help resources being tested during the study will not be freely available after the study period. However, the researchers will share information on how to access these resources for a fee after the study period to all participants. In addition to the time above, the researchers will collect information from participant's medical records for another 10 months after participation. The entire study is expected to last about 2 years.

Interventions

BEHAVIORALMoodkit

MoodKit is divided into four main sections: Activities, Thoughts, Mood and Journal. In the Thoughts section, the user is asked to briefly describe stressful situations and their reactions to the event and is later educated on a number of thought distortions. In the Mood section, the user is asked to give an overall rating of mood, which can be done several times per day. In the Journal section, the user can write freestanding journal entries. Additional areas of advice and goal setting are contained in a section called Thrive Tips.

BEHAVIORALMoodgym

The program consists of five modules each taking 20- to 40-minutes to complete, which are completed in a prescribed order.

BEHAVIORALUniversity of Michigan Depression Center Toolkit

The Toolkit provides information, tools, support, and resources to guide individuals through their mental health journey.

Sponsors

University of Michigan
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

This is a single-center, non-randomized, preferred assignment study.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Individuals who are English-speaking * Individuals with a Patient Health Questionnaire 9 (PHQ9) score greater than or equal to 11 or diagnosis of moderate to severe depression determined by the Care Manager during her initial psychiatric evaluation and by the study PI during panel review will supersede a low PHQ9 score. * Individuals with have daily internet access and a smartphone; * Individuals who agree to periodic contact with the care manager and study team.

Exclusion criteria

* Individuals who have cognitive impairment that would preclude use of self-help resources * Individuals with already using an electronic mental health resource; * Individuals with unstable medical illness, e.g. active cancer; * Individuals with severe psychiatric symptoms (marked suicidality, psychotic symptoms, severe substance abuse)

Design outcomes

Primary

MeasureTime frameDescription
Patient preference, use and satisfaction of the intervention as assessed by timed structured surveyUp to 14 months
Patient frequency and duration of intervention use and satisfaction as assessed by weekly structured surveyUp to 14 monthsStructured survey conducted weekly.
Patient preference and satisfaction with the intervention as assessed by qualitative interviewsUp to approximately 14 monthsInterviews are semi-structured and audio recorded
Care manager experiences of the intervention as assessed by qualitative interviewsUp to approximately 18 monthsInterviews are semi-structured and audio recorded
Clinician/Administrator views related to interventions as assessed by qualitative interviewsUp to approximately 18 monthsInterviews are semi-structured and audio recorded
Patient frequency of intervention use as assessed by self-report use of toolsUp to 14 monthsAs recorded in participants' printed copy of their mood-logs from the app or program.
Change in severity of symptoms of depression as assessed with the Patient Health Questionnaire 9 (PHQ-9) scoreAt baseline (before choosing an intervention) and at week 6 (when they complete the intervention)The PHQ-9 is an instrument for screening, diagnosing, monitoring and measuring the severity of depression: The PHQ-9 has a range of scores from 0-27. Depression Severity: 0- none, 1-4 minimal, 5-9 mild, 10-14 moderate, 15-19 moderately severe, 20-27 severe.
Change in level of functioning as assessed with the Sheehan Disability Scale (SDS)At baseline (before choosing an intervention) and at week 6 (when they complete the intervention)The Sheehan Disability Scale (SDS) is a 5-item clinician-rated questionnaire used to evaluate impairments in the domains of work, social life/leisure, and family life/home responsibility. All items are rated on a continuum (0 = no impairment to 10 = most severe) with the total SDS score ranging from 0 (no impairment) to 30 (most severe)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026