Workplace HIIT: Feasibility and Preventive Effects of HIIT in the Real-World

NCT ID: NCT04065191

Last Updated: 2019-08-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

300 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-05-01

Study Completion Date

2022-04-30

Brief Summary

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The aim of this study is to investigate the effects of an extremely time-efficient high-intensity interval training program, performed over a period of six months in a real-world (workplace) setting, on cardiorespiratory fitness, cardiometabolic risk profile, and self-reported outcomes including perceived stress and subjective work ability in previously sedentary employees.

Detailed Description

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Conditions

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Primary Prevention Health Promotion

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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High-intensity interval training

High-intensity interval training

Group Type EXPERIMENTAL

High-intensity interval training

Intervention Type OTHER

Heart rate based high-intensity interval training

Interventions

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High-intensity interval training

Heart rate based high-intensity interval training

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Sedentary Lifestyle over at least 1 year prior to the study

Exclusion Criteria

* Pregnancy, Lactation
* Psychological disorders, epilepsy, sever neurological disorders
* Participation in other exercise- or nutrition studies within the last 6 months
* coronary heart disease, heart failure
* malignant disease
* severe rheumatic or neurological disease
* severe/unstable hypertension (resting RR: \>180/\>110 mmHg)
* severely restricted lung function (FEV1 \<60%)
* unstable Diabetes mellitus
* severe orthopedic disease/restriction
* acute / chronic infectious diseases
* Electronic implants (defibrillator, pacemaker)
* Persons in mental hospitals by order of authorities or jurisdiction
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Erlangen-Nürnberg Medical School

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Dejan Reljic, Dr.

Role: PRINCIPAL_INVESTIGATOR

University Erlangen Nuremberg Medical School

Yurdaguel Zopf, Prof.

Role: PRINCIPAL_INVESTIGATOR

University Erlangen Nuremberg Medical School

Locations

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Department of Medicine 1, Hector Center for Nutrition, Exercise and Sports, Friedrich-Alexander-University Erlangen-Nuremberg

Erlangen, , Germany

Site Status RECRUITING

Countries

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Germany

Central Contacts

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Dejan Reljic, Dr.

Role: CONTACT

+49 9131 8545218

Yurdaguel Zopf, Prof.

Role: CONTACT

+49 9131 8545218

Facility Contacts

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Dejan Reljic, Dr.

Role: primary

+49 9131 8545218

Yurdaguel Zopf, Prof.

Role: backup

+49 9131 8545218

Other Identifiers

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WORK-HIIT-Study

Identifier Type: -

Identifier Source: org_study_id

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