Skip to content

Northern Board Beet Breathlessness Trial

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01610024
Enrollment
8
Registered
2012-06-01
Start date
2012-08-31
Completion date
2013-11-30
Last updated
2013-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Exercise Tolerance (Measured in Minutes)

Brief summary

Hypothesis: Beetroot juice increases the exercise tolerance of patients with chronic lung disease. Using the already established pulmonary rehabilitation model, we aim to split the group of 8 into 2 groups, each group taking 500ml of beetroot juice 24 hours before there class on alternate (differing) weeks to see if it improves their overall exercise tolerance.

Interventions

DIETARY_SUPPLEMENTBeetroot Juice

Give subjects 500ml beetroot juice in the 24 hour period prior to class begins. They will receive this during 3 of the 6 weeks

Sponsors

Northern Health and Social Care Trust
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Masking
DOUBLE (Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Already planned to attend the pulmonary rehabilitation class

Exclusion criteria

* Angina Prescribed regular nitrates, a resting heart rate \>100bpm, a resting blood pressure \<110 systolic, postural hypotension, prescribed PDE5 inhibitors.

Design outcomes

Primary

MeasureTime frameDescription
Exercise Tolerance6 weeksMeasuring incremental change in exercise tolerance between weeks of beetroot consumption and weeks of no beetroot consumption

Countries

United Kingdom

Contacts

Primary ContactWendy Anderson, MBBCh
Wendy.Anderson@northerntrust.hscni.net0044 2894424000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026