- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT03167658
The Impact of Employee Wellness Programs
7 septembre 2021 mis à jour par: Zirui Song, Harvard School of Public Health (HSPH)
There is great public and private interest in the use of workplace wellness programs to reduce health care spending, improve health outcomes, and enhance productivity for employees.
However, there is little rigorous evidence on the effects of wellness programs.
This study partners with a large multi-state U.S. employer (BJ's Wholesale Club) and an experienced wellness vendor (Wellness Workdays) to evaluate a multi-prong workplace wellness program, including components such as nutrition counseling, fitness challenges, and stress management workshops.
The wellness program will be delivered by a team of experts including Registered Dieticians, and will include financial rewards for participation.
The program will be available to employees in initially 20 of BJ's 200 worksites, and later expanded to 25 worksites.
These worksites have been randomly selected, allowing a randomized controlled trial evaluation of the effects of the wellness program.
Data will be collected on a wide array of outcomes from multiple sources, including on-site biometric screenings and surveys, employment records, and health insurance claims for employees at both treatment and control worksites.
Aperçu de l'étude
Statut
Complété
Les conditions
Intervention / Traitement
Type d'étude
Interventionnel
Inscription (Réel)
48664
Phase
- N'est pas applicable
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
18 ans et plus (Adulte, Adulte plus âgé)
Accepte les volontaires sains
Non
Sexes éligibles pour l'étude
Tout
La description
Inclusion Criteria:
- Employed in one of BJ's clubs during the period of the intervention
Exclusion Criteria:
- Not employed in one of BJ's clubs during the period of the intervention
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Autre
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
---|---|
Expérimental: Treatment
Employees at treatment worksites will be given access to workplace wellness programming.
Participation by employees will be voluntary, but all employees at treatment sites will be considered as part of the treatment group.
Employees will also be invited to complete on-site biometric assessments and questionnaires.
Data from secondary data sources (including employment records and health insurance claims) will be collected for employees at all BJ's worksites.
|
Multi-prong workplace wellness program, with components such as nutrition counseling, fitness challenges, and stress management workshops, including supports and incentives.
|
Aucune intervention: Primary Control
Employees at primary control worksites will be invited to complete on-site biometric assessments and questionnaires, but will not have access to the workplace wellness programming.
Data from secondary data sources (including employment records and health insurance claims) will be collected for employees at all BJ's worksites.
|
|
Aucune intervention: Secondary Control
Employees at secondary control worksites will not participate in in-person screenings or questionnaires, and will not have access to workplace wellness programming.
Data from secondary data sources (including employment records and health insurance claims) will be collected for employees at all BJ's worksites.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
Physical activity
Délai: Primary data collected at 18 months and 30 months after initiation of intervention
|
Regular exercise, number of hours sitting per day, and actively managing weight, as indicated in responses to survey questions
|
Primary data collected at 18 months and 30 months after initiation of intervention
|
Obesity
Délai: Primary data collected at 18 months and 30 months after initiation of intervention
|
Body Mass Index>=30, calculated from measured height and weight
|
Primary data collected at 18 months and 30 months after initiation of intervention
|
Absenteeism
Délai: Administrative records from 3 years spanning intervention
|
Number of sick or personal days as a share of total days employed, from employment records
|
Administrative records from 3 years spanning intervention
|
Health care spending
Délai: Administrative records from 3 years spanning intervention
|
Dollars spent on health care for employees covered by employer-sponsored insurance, from claims records
|
Administrative records from 3 years spanning intervention
|
Autres mesures de résultats
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
Blood pressure
Délai: Primary data collected at 18 months and 30 months after initiation of intervention
|
Systolic blood pressure, measured
|
Primary data collected at 18 months and 30 months after initiation of intervention
|
Depression
Délai: Primary data collected at 18 months and 30 months after initiation of intervention
|
Unmanaged depression, as indicated in responses to survey questions
|
Primary data collected at 18 months and 30 months after initiation of intervention
|
Tenure
Délai: Administrative records from 3 years spanning intervention
|
Duration of employment in days, from employment records
|
Administrative records from 3 years spanning intervention
|
Job performance
Délai: Administrative records from 3 years spanning intervention
|
Numerical performance rating from annual review, from employment records
|
Administrative records from 3 years spanning intervention
|
Health care spending (i.e. dollars spent)
Délai: Administrative records from 3 years spanning intervention
|
Dollars spent on health care and prescription drugs for employees covered by employer-sponsored insurance, decomposed into spending on inpatient, outpatient, emergency department, and prescription drugs, from claims records
|
Administrative records from 3 years spanning intervention
|
Health care utilization (i.e. number of doctor visits, hospitalizations, or medications)
Délai: Administrative records from 3 years spanning intervention
|
Health care encounters and prescription drugs for employees covered by employer-sponsored insurance, decomposed into inpatient, outpatient, emergency department, and prescription drugs, from claims records
|
Administrative records from 3 years spanning intervention
|
Nutrition management
Délai: Primary data collected at 18 months and 30 months after initiation of intervention
|
Affirmative engagement in active efforts to improve nutrition, as indicated in responses to survey questions
|
Primary data collected at 18 months and 30 months after initiation of intervention
|
Stress management
Délai: Primary data collected at 18 months and 30 months after initiation of intervention
|
Unmanaged stress and stress at work, as indicated in responses to survey questions
|
Primary data collected at 18 months and 30 months after initiation of intervention
|
Screenings and exams
Délai: Primary data collected at 18 months and 30 months after initiation of intervention
|
Percent of recommended tests received, as indicated in responses to survey questions
|
Primary data collected at 18 months and 30 months after initiation of intervention
|
Tobacco use
Délai: Primary data collected at 18 months and 30 months after initiation of intervention
|
Smoking, as indicated in responses to survey questions
|
Primary data collected at 18 months and 30 months after initiation of intervention
|
Health and wellbeing
Délai: Primary data collected at 18 months and 30 months after initiation of intervention
|
Short form 8 (SF-8) physical and mental summary scores, as indicated in responses to survey questions.
Each question of the SF-8 uses a 5- or 6-point Likert scale.
Its standardized scoring system combines responses into a score that can be interpreted as a continuous variable (analogous to a 0-100 scale), with higher scores denoting better self-reported health.
|
Primary data collected at 18 months and 30 months after initiation of intervention
|
Blood glucose
Délai: Primary data collected at 18 months and 30 months after initiation of intervention
|
Blood glucose, measured
|
Primary data collected at 18 months and 30 months after initiation of intervention
|
Cholesterol
Délai: Primary data collected at 18 months and 30 months after initiation of intervention
|
Total cholesterol and high-density lipoprotein (HDL), measured
|
Primary data collected at 18 months and 30 months after initiation of intervention
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Collaborateurs
Les enquêteurs
- Chercheur principal: Zirui Song, MD, PhD, Harvard Medical School (HMS and HSDM)
Publications et liens utiles
La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Réel)
1 janvier 2015
Achèvement primaire (Réel)
1 octobre 2018
Achèvement de l'étude (Réel)
1 juin 2021
Dates d'inscription aux études
Première soumission
23 mai 2017
Première soumission répondant aux critères de contrôle qualité
24 mai 2017
Première publication (Réel)
30 mai 2017
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
9 septembre 2021
Dernière mise à jour soumise répondant aux critères de contrôle qualité
7 septembre 2021
Dernière vérification
1 septembre 2021
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- Wellness 14-3141
- R01AG050329 (Subvention/contrat des NIH des États-Unis)
- P30AG012810 (Subvention/contrat des NIH des États-Unis)
- 72611 (Autre subvention/numéro de financement: Robert Wood Johnson Foundation)
- AEARCTR-0000586 (Identificateur de registre: American Economic Association Trial Registry)
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
NON
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Non
Étudie un produit d'appareil réglementé par la FDA américaine
Non
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .
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