Effects of Personal Technology Driven Workplace Wellbeing Intervention Programme on Wellbeing, Productivity (Presenteeism) and Absenteeism - an Intervention Study

NCT05274529 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 571

Last updated 2024-03-05

No results posted yet for this study

Summary

In this study the effects of a technology-driven workplace wellbeing intervention programme on employees' wellbeing, productivity (presenteeism) and absenteeism will be studied with the help of mobile applications and remotely conducted questionnaires, different wellbeing intervention periods and HRV based measurements.

Conditions

  • Occupational Stress
  • Occupational Burnout

Interventions

BEHAVIORAL

Psychological health and flexibility

A remote coaching programme concentrating on psychological health and flexibility

BEHAVIORAL

Work ability

A remote coaching programme concentrating on work ability

BEHAVIORAL

Sleep and recovery

A remote coaching programme concentrating on sleep and recovery

BEHAVIORAL

Healthy lifestyle

A remote coaching programme concentrating on healthy lifestyle

OTHER

No coaching

Participants also have the option to choose no coaching for the coming 3 month period.

Sponsors & Collaborators

  • Aisti Health Oy

    collaborator UNKNOWN
  • University of Jyvaskyla

    collaborator OTHER
  • Tampere University

    collaborator OTHER
  • Firstbeat Technologies Oy

    lead INDUSTRY

Principal Investigators

  • Jari Parkkari, Dr · Professor at University of Jyväskylä

  • Tero Myllymäki, M.Sc. · Head of Physiology Research at Firstbeat Technologies

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-04-12
Primary Completion
2026-10-31
Completion
2026-10-31

Countries

  • Finland

Study Locations

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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 NCT05274529 on ClinicalTrials.gov