Ignite Creation Date:
2024-05-06 @ 3:28 PM
Last Modification Date:
2024-10-26 @ 1:50 PM
Study NCT ID:
NCT04649528
Status:
COMPLETED
Last Update Posted:
2020-12-02
First Post:
2020-11-19
Brief Title:
HIIT for Inflammatory Rheumatic Disease Man vs Machine
Sponsor:
Molde University College
Organization:
Molde University College
Study Overview
Official Title:
Digitally Assisted High-intensity Interval Training in Inflammatory Rheumatic Disease Patients Treatment by Man or Machine
Status:
COMPLETED
Status Verified Date:
2020-11
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this study is to compare two modes of delivering high-intensity interval training HIIT in a population with inflammatory rheumatic disease over 10 weeks One group will recieved HIIT supervised by a healthcare professional the other group will perform self-monitored HITT with guidance by a smarthpone application
Detailed Description:
People with inflammatory rheumatic diseases IRS such as rheumatoid arthritis RA spondyloarthritis SpA and systemic lupus erythematosus SLE have been shown to have reduced cardiovascular fitness and quality of life than the general population Cardiovascular health is the single most important factor of total mortality It has been shown previously that individuals with IRS tolerate both endurance training resulting in improvement in function and cardiovascular health while also having a positive effect on disease activity measured through inflammation pain joint health and fatigue In recent years studies have also been conducted that demonstrate both the safety and effect of aerobic 4x4min high-intensity interval training HIIT for patients with IRS
This study will involve an intervention period consisting of 20 HIIT sessions Participants are randomized into one of two training groups One group will perform HIIT under the supervision of a healthcare professional The other group will perform the same HIIT training with identical instructions however they will be self-monitored with the aid and guidance of a mobilephone application
The purpose of the intervention is to increase maximum oxygen uptake and improve quality of life The intervention period will consist of 2 weekly sessions lasting approximately 35 minutes performed on non-consecutive days The endurance training will consist of 4 intervals of 4 minutes duration separated by a 3-4 minute active break and follows the principle of intensive aerobic interval training Before and after the training period identical testing approximately 30-40 min will be performed by both intervention groups The testing will include measurements of work economy and maximal oxygen uptake in an endurance test Additionally quality of life questionnaires will be obtained
This study will involve an intervention period consisting of 20 HIIT sessions Participants are randomized into one of two training groups One group will perform HIIT under the supervision of a healthcare professional The other group will perform the same HIIT training with identical instructions however they will be self-monitored with the aid and guidance of a mobilephone application
The purpose of the intervention is to increase maximum oxygen uptake and improve quality of life The intervention period will consist of 2 weekly sessions lasting approximately 35 minutes performed on non-consecutive days The endurance training will consist of 4 intervals of 4 minutes duration separated by a 3-4 minute active break and follows the principle of intensive aerobic interval training Before and after the training period identical testing approximately 30-40 min will be performed by both intervention groups The testing will include measurements of work economy and maximal oxygen uptake in an endurance test Additionally quality of life questionnaires will be obtained
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None