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Be Well at Work-Plus: A Depression and Physical Activity Intervention for Hospital Service Workers (Aim 3) 60 Randomisé

Pas encore en recrutement
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L'essai clinique NCT07010133 est une étude interventionnel pour Dépression, Inactivité physique. Son statut actuel est : pas encore en recrutement. Le recrutement est prévu pour commencer le 15 février 2026, avec un objectif de 60 participants. Dirigée par l'Université d'État de San Diego, l'étude devrait être terminée d'ici le 31 janvier 2027. Les données du site ClinicalTrials.gov ont été mises à jour pour la dernière fois le 11 février 2026.
Résumé succinct
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...Afficher plus
Description détaillée
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 ...Afficher plus
Titre officiel

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

Pathologies
DépressionInactivité physique
Autres identifiants de l'étude
Numéro NCT
NCT07010133
Date de début (réel)
2026-02-15
Dernière mise à jour publiée
2026-02-11
Date de fin (estimée)
2027-01-31
Inscription (estimée)
60
Type d'étude
Interventionnel
PHASE
N/A
Statut
Pas encore en recrutement
Mots clés
Depression
Physical Activity
Employees
Worker Health
Low-income
Social needs
Objectif principal
Traitement
Méthode d'allocation
Randomisé
Modèle d'intervention
Groupe unique
Masquage
Aucun (ouvert)
Bras / Interventions
Groupe de participants/BrasIntervention/Traitement
ExpérimentalImmediate 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.
Comparateur actifWaitlist 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.
Critère principal d'évaluation
Critères d'évaluationDescription de la mesurePériode
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).
Critère secondaire d'évaluation
Critères d'évaluationDescription de la mesurePériode
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)
Assistant à la participation
Critères d'éligibilité

Âges éligibles
Adulte, Adulte âgé
Âge minimum
18 Years
Sexes éligibles
Tous
  • 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 logoUniversité d'État de San Diego
National Heart, Lung, and Blood Institute (NHLBI) logoInstitut national du cœur, du poumon et du sang, États-Unis747 essais cliniques actifs à explorer
Contact central de l'étude
Contact: Jessica L McCurley, PhD, MPH, 619-594-2132, [email protected]
1 Centres de l'étude dans 1 pays

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, Investigateur principal