Remote vs. In-Person Study Evaluation (RISE) Trials: RISE Above Depression (Trial 2 of 3)

Part of paid clinical trials in Charleston, South Carolina.

Sponsor
State University of New York at Buffalo
Study ID
NCT07854301
Status
Not Yet Recruiting

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Conditions

  • In-person Visits
  • Remote Visits
  • Remote vs. In-Person

Eligibility Criteria

Sex
ALL
Age
18 Years - 99 Years
Healthy Volunteers
Accepted

Interventions

  • mobile health application (Moodivate) — BEHAVIORAL
    All participants receive the mobile health application "Moodivate".

Study Details

The study will employ a randomized, parallel-group design with two-stage randomization. After an initial brief screen for basic eligibility, participants will be randomized (within site) to either Remote (R) or In-Person (IP) Intake Groups. During the Intake, detailed consent and eligibility assessment will be completed. Participants who are eligible at the Intake will be randomized (within site and Intake Group) to R or IP Treatment and Assessment Groups. Participants will be followed for 3 months.

Key Dates

First listed
Oct 2, 2026
Start date
Oct 31, 2026
Status verified
Sep 2026
Primary completion
May 31, 2028
Completion
May 31, 2028

Study Design

Enrollment
100 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER

Arms

  • Other: REMOTE intake AND REMOTE treatment/assessment
    In this arm, ppts have been randomly assigned to a REMOTE INTAKE eligibility/baseline visit, and subsequently randomized to 5 REMOTE treatment/assessment visits.
  • Other: REMOTE intake BUT IN-PERSON treatment/assessment
    In this arm, ppts have been randomly assigned to a REMOTE INTAKE eligibility/baseline visit, and subsequently randomized to 5 IN-PERSON treatment/assessment visits.
  • Other: IN-PERSON intake, BUT REMOTE treatment/assessment
    In this arm, ppts have been randomly assigned to an IN-PERSON INTAKE eligibility/baseline visit, and subsequently randomized to 5 REMOTE treatment/assessment visits.
  • Other: IN-PERSON intake AND IN-PERSON treatment/assessment
    In this arm, ppts have been randomly assigned to an IN-PERSON INTAKE eligibility/baseline visit, and subsequently randomized to 5 IN-PERSON treatment/assessment visits.

Primary Outcome Measure

Accrual efficiency/Pre-treatment visits [ Time Frame: ~1 month ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Medical University of South CarolinaCharlestonSouth Carolina29425-

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By research site
Medical University of South Carolina· Charleston, SC

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