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Optimisation of ASthma In Those With Uncontrolled Symptoms (OASIS)

G

Guy's and St Thomas' NHS Foundation Trust

Status

Completed

Conditions

Asthma Attack
Asthma Persistent
Asthma
Covid19

Treatments

Device: ReferID

Study type

Interventional

Funder types

Other
Industry

Identifiers

Details and patient eligibility

About

A digital tool, called ReferID has been developed to facilitate the review of asthma patients. It aims to assist in the identification of patients with uncontrolled and/or severe asthma and to ensure a timely referral to secondary care where appropriate. To validate the tool, patients will be randomised to have a review with a healthcare professional using tool to facilitate the review or to continue receiving usual care. Outcome measures including exacerbation frequency and level of asthma control will be assessed at 12 months.

Enrollment

202 patients

Sex

All

Ages

18 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • All asthma patients with 1 of more exacerbations in the last 12 months or receiving high dose inhaled corticosteroids.
  • Patients able and willing to provide informed consent.
  • Patients aged 18 and over.

Exclusion criteria

  • Patients who lack capacity.
  • Patients who do not have a diagnosis of asthma
  • Patients who are unable to provide informed consent
  • Patients under the age of 18
  • Patients already under a severe asthma centre

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

202 participants in 2 patient groups

Healthcare professional using ReferID Tool in primary care
Active Comparator group
Description:
The asthma review will be undertaken by a healthcare professional with the use of the ReferID tool in primary care
Treatment:
Device: ReferID
Usual care in primary care
No Intervention group
Description:
A cohort of patients will be recruited who continue to receive usual care in primary care

Trial contacts and locations

1

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Central trial contact

Gill Arbane; Hetal Druve

Data sourced from clinicaltrials.gov

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