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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01765816
Other study ID # Gen-100-sub1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 2012
Est. completion date November 2014

Study information

Verified date September 2020
Source Norwegian University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Hypothesis: Exercise will reduce morbidity and mortality rates in an elderly population. The extent of reduction will be intensity dependent.

As part of the "Generation 100" study, this sub-study project will investigate the effect of exercise on blood volume, cardiopulmonary health and heart function in healthy aging. Objective is to determine the acute effect of one endurance training session on blood volume in healthy elderly. The working hypothesis is that one interval training session increases total blood volume by 10% in healthy elderly, and that there will be no change after moderate continuous training.


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date November 2014
Est. primary completion date February 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 70 Years to 75 Years
Eligibility Inclusion Criteria:

- ability to walk at least 1km,

- born in 1938,1939,1940,1941 or 1942

- Sufficiently good health to be able to take part in the study, as determined by the researchers

Exclusion Criteria:

- Illness or disability that precludes exercise or hinders completion of the study

- Uncontrolled hypertension

- Symptomatic valve disease, hyper tropic cardio-myopathy or unstable angina

- Active cancer

- Test results indicating that study participation is unsafe

- Inclusion in other studies conflicting with participation in this one

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
high intensity interval training

moderate intensity training


Locations

Country Name City State
Norway Norwegian University of Science and Technology Trondheim

Sponsors (1)

Lead Sponsor Collaborator
Norwegian University of Science and Technology

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary total blood volume carbon monoxide-rebreathing spirometry (Bayreuth, Germany) 24 hours
Secondary hemoglobin volume carbon monoxide-rebreathing spirometry (Bayreuth, Germany) 24 hours
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