Exercise Training on Metabolic Syndrome Severity in Employees

Hannover Medical School (MHH)

Status: Completed

Conditions: Metabolic Syndrome

Treatments: Behavioral: Exercise training group

Study type: Interventional

Funder types: Other

Identifiers

NCT03293264

RebVW

Details and patient eligibility

About

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..

Enrollment: 314 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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314 participants in 2 patient groups

Exercise training group

Experimental group

Description:

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.

Treatment:

Behavioral: Exercise training group

Waiting-control group

No Intervention group

Description:

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.