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Clinical Trials/NCT03293264
NCT03293264CompletedNot Applicable

Effects of a Workplace Health Service Program in Employees With Diagnosed Metabolic Syndrome

Hannover Medical School1 site in 1 country314 target enrollmentStarted: October 17, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
314
Locations
1
Primary Endpoint
Change from baseline in Metabolic Syndrome (MetS) -Z-score

Study Overview

Brief Summary

Hypothesis: An occupational 6 months physical exercise training will lead to better health behaviour and improve the severity of the metabolic syndrome.

312 subjects will be assigned to either an intervention or a waiting-control-group. The intervention group will receive instructions with the aim to perform 150 min exercise training per week. Exercise consists of endurance, strength and coordination training. A feedback system guided by sports scientists will be installed for all subjects in the intervention group using activity monitoring (wearable). After 6 months training subjects from the intervention group will be assigned to one of the following groups for follow-up observation from month 6 to months 12:

  • training with personal/individual feedback from sport scientist
  • training with automated feedback using activity monitoring Tools (wearable)
  • training without further feedback Subjects assigned to the control group will be provided with information on low intensity motion exercises. After 6 months in the control group subjects will be provided with the same exercise intervention as the intervention for a duration of 6 months.

Study visits will be conducted at month 0, month 6, month 12, and a long-term follow-up at month 24..

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
Single (Investigator)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •3 out of 5 parameters of the metabolic syndrome

Exclusion Criteria

  • •ongoing participation in occupational health service
  • •clinical relevant acute or chronic infections
  • •pregnancy
  • •surgery dating back less than 8 weeks
  • •artificial joint replacement dating back less than 6 months
  • •tumor disease dating back less than 5 years
  • •every other disease or relevant functional disorder not allowing to participate in regular physical exercise

Arms & Interventions

Exercise training group

Experimental

The intervention group will be encouraged to perform 150 min of exercise training per week for 6 months. Subjects will be provided with individual feedback and exercise Training prescriptions. After month 6 subjects will be randomized to three different groups for follow-up observation.

Intervention: Exercise training group (Behavioral)

Waiting-control group

No Intervention

The control group will be provided with general informations on a healthy lifestyle. After 6 months wait-list-control months subjects will receive the guided exercise training intervention for 6 months.

Outcomes

Primary Outcomes

Change from baseline in Metabolic Syndrome (MetS) -Z-score

Time Frame: 6 months 12 months, 24 months

Z-Score (arbitrary unit, ranging from -2 to 2), assessed and calculated from the 5 established components of the metabolic syndrome: triglycerides, HDL cholesterol, fasting glucose, waist circumference, and systolic blood pressure.

Secondary Outcomes

  • Change from baseline in Pmax(6 months)
  • Change from baseline in Anxiety- and depression severity(6 months, 12 months, 24 months)
  • Change from baseline in adherence to training program(6 months, 12 months, 24 months)
  • Change from baseline in Work-Ability-Index (WAI)(6 months, 12 months, 24 months)
  • Change from baseline in Body weight(6 months)
  • Change from baseline in Health-related quality of live: score of SF36 questionnaire(6 months, 12 months, 24 months)
  • Change from baseline in body composition(6 months, 12 months, 24 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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