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DepressionOHDC-DCNCT06206226

The Oh Happy Day Class - Digital Connections (OHDC-DC): A Pilot Study

A study testing OHDC-DC in people with Depression and Depressive Disorder, run by University of Wisconsin, Madison at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

The goal of this clinical trial is to see if a mobile phone app can deliver depression treatment to African Americans who are depressed. The main question it aims to answer is if this treatment is effective in reducing symptoms of depression. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
OHDC-DC
Could I receive a placebo?
No, everyone receives an active treatment
How many people
8 participants
Where
1 siteUnited States
Study dates
Oct 2026to Feb 2027
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • African-American
  • Age 18 and older
  • Experiencing depression (as evidenced by a score of 5 or higher on the PHQ-9)
  • Own a mobile phone

Who cannot join

  • Individuals who are currently receiving psychotherapy
  • Individuals who are presently experiencing suicidal ideation
  • Individuals who started psychotropic medication less than three months prior to the start of the OHDC will be excluded from the study
  • Participants scoring 25 or higher on the PHQ-9 will be screened out

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

United States1 site, 1 recruiting
  • University of Wisconsin

    Madison, Wisconsin, 53705

    Shari Barlow, 608-265-4348, shari.barlow@fammed.wisc.edu

    Earlise Ward, PhD

    Recruiting

Other trials in United States

About this study

Official title: The Oh Happy Day Class - Digital Connections (OHDC-DC): an Exploratory Pilot Study

The goal of this clinical trial is to see if a mobile phone app can deliver depression treatment to African Americans who are depressed. The main question it aims to answer is if this treatment is effective in reducing symptoms of depression.

Participants will attend six 90-minute weekly classes via an app on their phone, and will be asked to complete surveys every week. Participants can expect to be in the study for four months.

Read the detailed description

The Oh Happy Day Class-Digital Connections (OHDC-DC) is designed for African American adults experiencing clinical depression (CD). OHDC originally comprised of 13 treatment modules focused on culturally relevant strategies to increase knowledge of depression and healthy coping behaviors aimed at reducing symptoms of clinical depression and improving health outcomes.

The Oh Happy Day Class-Digital Connections (OHDC-DC) comprise of 5 core elements of the OHDC-DC:

  1. 90-minute-weekly cognitive behavioral psycho-education classes over a 6-week period.
  2. Six classes will be offered and facilitated online in the computerized OHDC-DC.
  3. Participants will be encouraged to stay engaged between classes by digitally connecting on the app with the class content. On the app they will receive reminders and messages from staff and participants to stay digitally connected and engaged.
  4. Embedded in the classes and content is psychoeducation with an emphasis on educating participants about depression, raising awareness of mental illness with the goal of normalizing it and reducing stigma, and increasing healthy coping behaviors, and.
  5. The intervention will be delivered by a licensed mental health clinician.
Being tested
OHDC-DC
Keywords
African American
Medical subject headings
Depression, Depressive Disorder

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • OHDC-DCBehavioural

    90-minute-weekly cognitive behavioral psycho-education classes using a mobile phone app over a 6-week period

Study groups in NCT06206226
Study groupRoleWhat they receive
Oh Happy Day Class-Digital Connections (OHDC-DC)ExperimentalNot described
Receives: Behavioral: OHDC-DC

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Personal Health Questionnaire Depression Scale score

    Using the 8 item Personal Health Questionnaire Depression Scale (PHQ-8), participants will rate how much they have been bothered by symptoms on a scale of 0-3 with a possible range of 0 to 24. Higher scores indicate greater degree of depression.

    Measured: Baseline to one month post-intervention (approximately 12 weeks)

  2. Change in Generalized Anxiety Disorder 7-item (GAD-7) score

    Using the GAD-7 score, participants will rate how much they have been bothered by symptoms on a scale of 0-3 with a possible range of 0 to 24. Higher scores indicate greater degree of anxiety.

    Measured: Baseline to one month post-intervention (approximately 12 weeks)

  3. Change in Quick Inventory of Depressive Symptomatology (QIDS)

    Using the 16-item QIDS, participants will rate how much they have been bothered by symptoms on a scale of 0-3 with a possible range of 0 to 27. Higher scores indicate greater degree of depression.

    Measured: Baseline to one month post-intervention (approximately 12 weeks)

  4. Satisfaction with intervention

    Participants will rate their satisfaction with the intervention by answering a 9-item questionnaire with a scale of 1-7 (1= none of the time, 7= all of the time). Higher scores indicate greater satisfaction with the intervention.

    Measured: 12 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Jan 2024
  2. Study startOct 2026 (estimated)
  3. Primary completionFeb 2027 (estimated)
  4. Study completionFeb 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
8 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06206226
Sponsor's protocol ID
2023-1437
Other IDs
A532007, SMPH/FAMILY MED/RES GRANTS, Protocol Version 11/16/23
Acronym
OHDC-DC
Status last verified
Sep 2026
First submitted
4 Jan 2024
Last updated
29 Sep 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

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