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NCT05343949

High Intensity Interval Training and Technologies in COPD

Terminated NA Last updated 11 April 2024
What this trial tests

NA trial testing HIIT exercise program ABC in COPD in 18 participants. Terminated before completion.

Timeline
8 May 2019
Primary endpoint
25 November 2022
25 November 2022

Quick facts

Lead sponsorHull University Teaching Hospitals NHS Trust
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingsingle
Primary purposesupportive care
Enrollment18
Start date8 May 2019
Primary completion25 November 2022
Estimated completion25 November 2022
Sites1 location across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

Hull University Teaching Hospitals NHS Trust

Who can join

Adults 30 to 90, any sex, with COPD. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Trials in COPD have shown that HIIT leads to the same positive outcomes as constant load training but causes less breathlessness and leg discomfort during training. However, HIIT protocols in existing trials have all been different and use relatively long interval durations (30 s) and short rests. This is sub-optimal because long interval durations lead to greater breathlessness and patients may fear that they will not fully recover during short rests, potentially decreasing adherence. A novel HIIT protocol involving very brief intervals (e.g. 10 s) with longer rests may provide the same benefits with less distress due to breathlessness.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for COPD

Currently open trials in the same condition.

Other Hull University Teaching Hospitals NHS Trust trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05343949.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing