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Università statale di San DiegoBe Well at Work-Plus: A Depression and Physical Activity Intervention for Hospital Service Workers (Aim 3) 60 Randomizzato
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La sperimentazione clinica NCT07010133 è uno studio interventistico per Depressione, Inattività fisica, attualmente non ancora in arruolamento. L'arruolamento dovrebbe iniziare il 15 febbraio 2026, con l'obiettivo di raggiungere 60 partecipanti. Sotto la guida di l'Università statale di San Diego, dovrebbe concludersi entro il 31 gennaio 2027. I dati più recenti da ClinicalTrials.gov sono stati aggiornati l'ultima volta il 11 febbraio 2026.
Sommario breve
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...Mostra di più
Descrizione dettagliata
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 ...Mostra di più
Titolo ufficiale
Be Well at Work-Plus: A Depression and Physical Activity Intervention for Hospital Service Workers (Aim 3).
Patologie
DepressioneInattività fisicaAltri ID dello studio
Numero NCT
Data di inizio (effettiva)
2026-02-15
Ultimo aggiornamento pubblicato
2026-02-11
Data di completamento (stimata)
2027-01-31
Arruolamento (previsto)
60
Tipo di studio
Interventistico
FASE
N.D.
Stato
Non ancora in arruolamento
Parole chiave
Depression
Physical Activity
Employees
Worker Health
Low-income
Social needs
Physical Activity
Employees
Worker Health
Low-income
Social needs
Scopo principale
Trattamento
Allocazione
Randomizzato
Modello di intervento
A gruppo singolo
Mascheramento
Nessuno (studio in aperto)
Bracci / Interventi
| Gruppo/Braccio di partecipanti | Intervento/Trattamento |
|---|---|
SperimentaleImmediate 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. |
Comparatore attivoWaitlist 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. |
Esito primario
Esito secondario
| Misure di esito | Descrizione della misura | Arco temporale |
|---|---|---|
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). |
| Misure di esito | Descrizione della misura | Arco temporale |
|---|---|---|
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) |
Assistente alla partecipazione
Criteri di eleggibilità
Età idonea
Adulto, Adulto anziano
Età minima
18 Years
Sessi idonei
Tutti
- 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)
Università statale di San DiegoIstituto nazionale del cuore, dei polmoni e del sangue, Estados Unidos747 studi clinici attivi da esplorareContatti principali dello studio
Contatto: Jessica L McCurley, PhD, MPH, 619-594-2132, [email protected]
1 Centri dello studio in 1 paesi
California
San Diego State University, San Diego, California, 92115, United States
Jessica L McCurley, PhD, MPH, Contatto, 619-594-2132, [email protected]
Jessica L McCurley, PhD, MPH, Investigatore principale