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N/A N=70 Randomized Single-blind Treatment

A Systems-Level Intervention for Rural Adults With Depression

Depressive Symptoms

Enrolled (actual)
70
Serious AEs
0.0%
Results posted
Feb 2025
Primary outcome: Primary: Change in Self-report Measure of Depressive Symptoms — 13.90; 13.43; 7.00; 7.57 score on PHQ-9

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Raising Our Spirits Together (Behavioral); Enhanced Control Condition (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Michigan
Primary completion
Jul 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in Self-report Measure of Depressive Symptoms
13.90; 13.43; 7.00; 7.57; 7.72; 8.10

Summary

This study aims to test the effectiveness of a computer-assisted cognitive behavioral therapy for depression among rural adults. The intervention, called Raising Our Spirits Together (ROST), was developed via a community-based participatory approach and will be delivered in small groups, facilitated by local pastors. Groups will be held virtually, or in-person at two churches in rural Michigan. Eighty-four individuals will be recruited from Hillsdale, Michigan, to test the effect of ROST on depressive symptoms, compared to an Enhanced Control Condition (ECC).

Eligibility Criteria

Inclusion Criteria

  • Must live in Hillsdale, Lenawee, Jackson, or Calhoun County, Michigan
  • Positive screen for at least mild depressive symptoms based on the the Patient Health Questionnaire-9 (PHQ-9>=5)

Exclusion Criteria

  • Non-English speaking
  • Currently receiving cognitive behavioral therapy (CBT) for depression
  • Ever completed a course of cognitive behavioral therapy (CBT; >=8 sessions)
  • Diagnosis of a psychotic disorder
  • Current use of opiates or freebase cocaine
  • Prominent suicidal/homicidal ideation with imminent risk.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04502186). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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