Effect of 3 Years of Exercise on Development of Atrial Fibrillation

NCT ID: NCT01680302

Last Updated: 2022-09-19

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

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

1567 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-09-30

Study Completion Date

2026-06-30

Brief Summary

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This is a substudy of "Generation 100". In that study, 4000 healthy persons between 70 and 75 will be randomised to a moderate intensity training group, a high intensity training group or control group, with 3 years of exercise. The investigators will follow these persons and register all who develop atrial fibrillation during these 3 years, and at follow-up after ended intervention to see if there is differences in the number of persons who develop atrial fibrillation in the 3 groups.

Detailed Description

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Conditions

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Atrial Fibrillation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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High intensity exercise

High intensity exercise(Borg 16) in intervals.

Group Type EXPERIMENTAL

High intensity exercise

Intervention Type BEHAVIORAL

Moderate intensity exercise

Moderate intensity exercise 3 times a week.

Group Type EXPERIMENTAL

Moderate intensity exercise

Intervention Type BEHAVIORAL

Control group

Exercise on their own. Follow current guidelines.

Group Type EXPERIMENTAL

Control

Intervention Type BEHAVIORAL

Advised to follow current guidelines for physical activity, but exercise on their own.

Interventions

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High intensity exercise

Intervention Type BEHAVIORAL

Moderate intensity exercise

Intervention Type BEHAVIORAL

Control

Advised to follow current guidelines for physical activity, but exercise on their own.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Participating in the "Generation 100" study

Exclusion Criteria

\-
Minimum Eligible Age

70 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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St. Olavs Hospital

OTHER

Sponsor Role collaborator

Norwegian University of Science and Technology

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Jan Paal Loennechen, PhD

Role: STUDY_CHAIR

St. Olavs Hospital

Locations

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Norwegian University of Science and Technology

Trondheim, , Norway

Site Status

Countries

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Norway

Other Identifiers

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2012/978b-2

Identifier Type: -

Identifier Source: org_study_id

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