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Not yet recruiting NCT07618312

Improving Patient Engagement in Mental Health Services

No phase Interventional Depression Disorder Engagement

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Behavioral Activation.
Who it may be relevant to
Registry conditions: Depression Disorder, Engagement. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Improving Patient Engagement in Mental Health Services: Adaptation and Implementation of a Behavioral Activation Intervention

Overview

Hybrid Type II Implementation Trial

Detailed description

The goal of this hybrid type II implementation trial is to test a telehealth behavioral activation intervention delivered in Spanish by community health workers in Spanish speakers living in rural and frontier areas of Montana and New Mexico. The main questions it aims to answer are:

Does an adapted behavioral activation intervention reduce depressive symptoms? Is engagement in the intervention the primary mechanism by which depressive scores are reduced?

Researchers will compare depressive symptoms in the intervention group as compared to a waitlisted group.

Participants will receive a weekly behavioral activation session via telehealth and will be asked to complete weekly surveys and homework. They will complete the Beck Depression Inventory (21 items) at baseline, after 12 weeks, and after 32 weeks.

Interventions

  • Behavioral Behavioral Activation
    Adapted version of BA intervention delivered via telehealth

Primary outcome measures

  • Beck Depression Inventory (21 items) [Time frame: Baseline, After 12 weeks, After 32 weeks]
Secondary outcome measures (1)
  • Behavioral Activation for Depression Scale Short Form, Session Attendance, Activation Homework [Time frame: weekly for 12 weeks]

Eligibility criteria

Inclusion criteria

  • Age 18 years or older
  • Spanish-speaking adult who prefers to receive services in Spanish

Resident of a rural or frontier community in Montana or New Mexico

Positive screen for depressive symptoms at or above study eligibility threshold on Spanish-language screening measure

Able and willing to participate in telehealth sessions

Able to provide informed consent

Exclusion criteria

  • Active suicidal intent requiring immediate emergency intervention

Current psychosis or mania

Severe cognitive impairment that would prevent participation

Currently receiving intensive psychiatric treatment that would conflict with the intervention

Unable to participate in telehealth sessions

Unable to provide informed consent

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Crossover
Masking
Open label
Primary purpose
Health services research

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07618312 · Moyce022026

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗