Be Well at Work-Plus: A Depression and Physical Activity Intervention for Hospital Service Workers (Aim 3)

Conditions

• Depression
• Physical Inactivity

Eligibility Criteria

Sex

ALL

Age

18 Years - N/A

Healthy Volunteers

Not accepted

Interventions

• A workplace-based depression intervention for low-wage hospital workers — BEHAVIORAL
  This intervention is a remotely delivered workplace-based depression intervention that is tailored to the specific social and behavioral needs of low-wage hospital service workers. The intervention involves assessment of depression-related work impairment, work-focused cognitive behavioral therapy, work coaching, social needs screening and referral, and text message support for mood and physical activity.

Study Details

This small randomized controlled trial will evaluate a workplace-based depression intervention that is tailored to the specific social and behavioral needs of low-wage hospital service workers. The intervention involves assessment of depression-related work impairment, work-focused cognitive behavioral therapy, work coaching, social needs screening and referral, and text message support for mood and physical activity.

Key Dates

Start date

Jun 1, 2026

Status verified

Apr 2026

Primary completion

Dec 31, 2026

Completion

Jan 31, 2027

Study Design

Enrollment

60 participants (estimated)

Allocation

RANDOMIZED

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Arms

• Experimental: Immediate Intervention
  The intervention consists of assessment of depression and work impairment, work-focused cognitive behavioral therapy, work coaching, social needs screening and referral, and text message support for mood and physical activity.
• Active Comparator: Waitlist Control
  Delivered after a 4-month waitlist period, the intervention consists of assessment of depression and work impairment, work-focused cognitive behavioral therapy, work coaching, social needs screening and referral, and text message support for mood and physical activity.

Primary Outcome Measure

Intervention feasibility [ Time Frame: From enrollment to end of treatment (approximately 4 months after enrollment). ]

Central Contacts

• Jessica L McCurley, PhD, MPH
  619-594-2132
  [email protected]

Locations (1)

Find similar trials in San Diego, CA

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