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

F

Firstbeat Technologies

Status

Active, not recruiting

Conditions

Occupational Stress
Occupational Burnout

Treatments

Other: No coaching
Behavioral: Work ability
Behavioral: Healthy lifestyle
Behavioral: Sleep and recovery
Behavioral: Psychological health and flexibility

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT05274529
Coachbeat

Details and patient eligibility

About

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.

Full description

The objectives of this study are:

  1. To study the effects of a data driven adaptive workplace wellbeing intervention programme on productivity (presenteeism) and absenteeism of the employees.
  2. To study the effects of data driven adaptive workplace wellbeing interventions on employees' physical health measures and wellbeing. The secondary objective also includes studying whether the programme generates measurable financial savings.

This study is an intervention study where eligible participants will be offered a technologically delivered health promotion intervention which is personalized to their needs both in terms of content and timing within the 12-month intervention period. The outcomes are compared against their pre-intervention levels at both individual and group level. The study has no control group as it is not acceptable for the participating companies to offer participation only to part of their employees based on randomization due to expected positive impact of the intervention. The lack of the control group will be taken into account while analyzing and interpreting the study results.

The 12-month intervention period consists of access to Firstbeat Life (HRV & movement measurement based wellbeing service), Aava Medical's Aisti wellbeing assessment and four types of online coaching programmes plus option of no coaching. Every participant has continuous access to Firstbeat Life and Aisti during the entire intervention programme and may use them at any time they so desire. In addition, participants will use the Coachbeat mobile app which is used to instruct and communicate with the participants, to fill in all the study questionnaires at given times, and to promote use of Firstbeat Life and Aisti at given points of the study. Baseline measurements and measurements after 4 and 8 months give recommendations for participation to the online coaching based on Firstbeat Life and Aisti wellbeing assessment. The participants can choose the coaching program based on the recommendation or their own interest. They can participate several coaching programmes during the study. Each coaching programme lasts approximately 3 months.

Enrollment

571 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

The initial target population consists of generally healthy employees of selected employer companies from information intensive industries and jobs.

Inclusion Criteria:

  • Signed written informed consent
  • Adequate Finnish or English1 language skills to comprehend study-related instructions and questionnaires. The services and contents are available only in Finnish and English.

Exclusion Criteria:

  • Planned absenteeism from work during the study with >3mth duration
  • Use of cardiac pacemaker or history of atrial fibrillation
  • No access to compatible mobile phone
  • History of a major cardiovascular event (myocardial infarction, coronary artery bypass graft (CABG), percutaneous coronary intervention (PCI), stroke, or transient ischemic attack) within the previous 6 months

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

571 participants in 1 patient group

Study group
Experimental group
Description:
All the participants will be in the same group and have the same intervention programmes options to choose from.
Treatment:
Behavioral: Psychological health and flexibility
Other: No coaching
Behavioral: Healthy lifestyle
Behavioral: Work ability
Behavioral: Sleep and recovery

Trial contacts and locations

1

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Central trial contact

Research Coordinator

Data sourced from clinicaltrials.gov

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