Long-term Impact Evaluation of a Worksite-based Lifestyle Intervention to Reduce Cardiovascular Risk in Office Workers

NCT02561065 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1020

Last updated 2021-04-28

No results posted yet for this study

Summary

The main objective of TANSNIP-PESA is to determine in a population of asymptomatic bank employees with high and low imaging defined cardiovascular disease (CVD) risk the effectiveness of a comprehensive 3-year worksite-based lifestyle intervention consisting of 12 personalized lifestyle counseling sessions, a Fitbit physical activity tracker and a sit-stand Workstation.

Conditions

Interventions

BEHAVIORAL

Lifestyle intervention

1. Each participant will receive 12 personalized lifestyle counseling sessions given face-to-face by a trained practitioner. 2. The Fitbit physical activity tracker gives summaries of the participant's physical activity, provides stimulating prompts and rewards, and allows for social media sharing and competition. 3. A Sit-stand workstation allows to adjust the height of the participant workstation, including the computer screen, keyboard and mouse and allows them to easily switch between sitting and standing throughout the workday.

Sponsors & Collaborators

  • Amsterdam UMC, location VUmc

    collaborator OTHER
  • Instituto de Salud Carlos III

    collaborator OTHER_GOV
  • Icahn School of Medicine at Mount Sinai

    collaborator OTHER
  • Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III

    lead OTHER

Principal Investigators

  • Valentin Fuster, MD, PhD · Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III

  • Jose Maria Castellano, MD, PhD · Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III

  • Hidde van der Ploeg, PhD · Amsterdam UMC, location VUmc

  • Willem van Mechelen, MD, PhD · Amsterdam UMC, location VUmc

  • Borja Ibañez, MD, PhD · Centro Nacional de Investigaciones Cardiovasculares Carlos III (F.S.P.)

  • Antonio Fernandez-Ortiz, MD, PhD · Centro Nacional de Investigaciones Cardiovasculares Carlos III (F.S.P.)

  • Ines García Lunar, MD, PhD · Centro Nacional de Investigaciones Cardiovasculares Carlos III (F.S.P.)

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-05-25
Primary Completion
2020-01-30
Completion
2020-01-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02561065 on ClinicalTrials.gov