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Clinical Trial NCT07010133 for Depression, Physical Inactivity is not yet recruiting. See the Trial Radar Card View and AI discovery tools for all the details. Or ask anything here.
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Be Well at Work-Plus: A Depression and Physical Activity Intervention for Hospital Service Workers (Aim 3) 60 Randomized

Not yet recruiting
Clinical Trial NCT07010133 is an interventional study for Depression, Physical Inactivity and is currently not yet recruiting. Enrollment is planned to begin on 15 February 2026 and continue until the study accrues 60 participants. Led by San Diego State University, this study is expected to complete by 31 January 2027. The latest data from ClinicalTrials.gov was last updated on 11 February 2026.
Brief Summary
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...Show More
Detailed Description
Depression and physical inactivity are leading contributors to cardiometabolic diseases such as obesity, diabetes, and cardiovascular disease. Low-wage workers, who comprise one third of all workers in the U.S. and are essential to many industries, are more likely to be physically inactive and to have cardiometabolic conditions and depression, yet the participants are half as likely as higher wage workers to utilize ...Show More
Official Title

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

Conditions
DepressionPhysical Inactivity
Other Study IDs
NCT ID Number
NCT07010133
Start Date (Actual)
2026-02-15
Last Update Posted
2026-02-11
Completion Date (Estimated)
2027-01-31
Enrollment (Estimated)
60
Study Type
Interventional
PHASE
N/A
Status
Not yet recruiting
Keywords
Depression
Physical Activity
Employees
Worker Health
Low-income
Social needs
Primary Purpose
Treatment
Design Allocation
Randomized
Interventional Model
Single Group
Masking
None (Open Label)
Arms / Interventions
Participant Group/ArmIntervention/Treatment
ExperimentalImmediate 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.
A workplace-based depression intervention for low-wage hospital workers
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.
Active ComparatorWaitlist 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.
A workplace-based depression intervention for low-wage hospital workers
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.
Primary Outcome Measures
Outcome MeasureMeasure DescriptionTime Frame
Intervention feasibility
Feasibility will be assessed by the number of intervention sessions completed. The intervention will be considered feasible if the majority of participants complete 75% (6 of 8) or more phone sessions.
From enrollment to end of treatment (approximately 4 months after enrollment).
Depression symptoms
Depression symptoms will be measured with the Patient Health Questionnaire - 9 item version (range 0-27, higher = worse depression symptoms)
From baseline through end of treatment (approximately 4 months after enrollment).
Secondary Outcome Measures
Outcome MeasureMeasure DescriptionTime Frame
Work limitations
Work limitations (range: 0-100%, higher = more limitation) will be measured by the Work Limitations Questionnaire.
From baseline to end of treatment (approximately 4 months after enrollment)
Perceived stress
Perceived stress measured by the Perceived Stress Scale (range 0-40, higher = more perceived stress).
From baseline to end of treatment (approximately 4 months after enrollment)
Sleep quality
Sleep quality and duration as measured by the Pittsburgh Sleep Quality Index (range: 0-21, higher scores indicate worse sleep quality).
Baseline, follow-up (4 months)
Physical activity - step count
Weekly step count as measured by wrist-worn FitBit watch
Baseline, follow-up (4 months)
Body Mass Index
A weight-to-height ratio, calculated by dividing participant's weight in kilograms by height in meters squared.
Baseline, follow-up (4 months)
Blood pressure
Resting systolic and diastolic blood pressures
Baseline, Follow-up (4 months)
Physical Activity (self-report)
Self-reported physical activity using the Global Physical Activity Questionnaire
Baseline, Follow-up (4 months)
Participation Assistant
Eligibility Criteria

Eligible Ages
Adult, Older Adult
Minimum Age
18 Years
Eligible Sexes
All
  • part-time or full-time employment (at least 20 hours per week);
  • ≥18 years old;
  • employed in low-wage-earning jobs in the Environmental Services or Food & Nutrition Services Departments;
  • presence of depression symptoms as measured by the Patient Health Questionnaire-9 item version; individuals who score ≥5 (indicating mild depression symptoms or higher) will be eligible;
  • presence of impairment in work functioning, as measured by the Work Limitations Questionnaire; individuals who score ≥5% (indicating mild work productivity loss) will be eligible;
  • possession of a cell phone with ability to receive text-messages;
  • Fluent in either English or Spanish.

  • plan to leave Scripps employment in <6 months;
  • severe mental illness or substance use condition (e.g., bipolar disorder, schizophrenia, active alcohol use disorder)
San Diego State University logoSan Diego State University
National Heart, Lung, and Blood Institute (NHLBI) logoNational Heart, Lung, and Blood Institute (NHLBI)747 active studies to explore
Study Central Contact
Contact: Jessica L McCurley, PhD, MPH, 619-594-2132, [email protected]
1 Study Locations in 1 Countries

California

San Diego State University, San Diego, California, 92115, United States
Jessica L McCurley, PhD, MPH, Contact, 619-594-2132, [email protected]
Jessica L McCurley, PhD, MPH, Principal Investigator