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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03229434
Other study ID # ARMH_2
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 29, 2017
Est. completion date November 1, 2017

Study information

Verified date January 2019
Source Universitaet Innsbruck
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In a randomized crossover design, approximately 50 healthy participants will be randomly exposed to outdoor mountain hiking (approximately 6 hours each) in two different areas: an anthropogenically influenced area and in a widely pristine area.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date November 1, 2017
Est. primary completion date November 1, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- voluntary participation

Exclusion Criteria:

- pregnancy

- breastfeeding

- chronic or acute diseases (already existing or diagnosed during the study)

- unable to be physically active assessed by the Physical Activity Readiness Questionnaire

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Mountain hiking
Compare arm description

Locations

Country Name City State
Austria Department of Sport Science, Medical Section, University of Innsbruck Innsbruck

Sponsors (2)

Lead Sponsor Collaborator
Universitaet Innsbruck Paracelsus Medical University

Country where clinical trial is conducted

Austria, 

References & Publications (1)

Niedermeier M, Einwanger J, Hartl A, Kopp M. Affective responses in mountain hiking-A randomized crossover trial focusing on differences between indoor and outdoor activity. PLoS One. 2017 May 16;12(5):e0177719. doi: 10.1371/journal.pone.0177719. eCollection 2017. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline Cortisol (Saliva Sampling) at 6 hours Physiological response 6 hours
Primary Change from baseline subscales of mood survey scale at 6 hours Psychological response 6 hours
Secondary Change from baseline blood pressure at 6 hours 6 hours
Secondary Change from baseline lung function at 6 hours 6 hours
Secondary Change from baseline respiratory gas analysis at 6 hours 6 hours
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