ISRCTN ISRCTN66284870
DOI https://doi.org/10.1186/ISRCTN66284870
Protocol serial number 06/039/SMI
Sponsor Brighton and Sussex University Hospitals NHS Trust (UK)
Funders Brighton and Sussex Medical School (UK) - originally held by from Southampton University, Alk-Abello Ltd (UK) (ref: D105 R107)
Submission date
25/04/2006
Registration date
06/06/2006
Last edited
08/02/2012
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Respiratory
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data

Plain English summary of protocol

Not provided at time of registration

Contact information

Prof Helen Smith
Scientific

Brighton and Sussex Medical School
Mayfield House
University of Brighton
Falmer
Brighton
BN1 9PH
United Kingdom

Phone +44 (0)1273 644563
Email h.e.smith@bsms.ac.uk

Study information

Primary study designInterventional
Study designRandomised controlled trial
Secondary study designRandomised controlled trial
Study type Participant information sheet
Scientific title
Study acronymSPT
Study objectivesDoes allergy assessment and appropriate advice in general practice enhance the care of patients with asthma and rhinitis and is it cost effective compared with routine medical care?
Ethics approval(s)Ethics approval received from the Multicentre Research Ethics Committee on the 26th May 2003 (ref: MREC/02/10/13).
Health condition(s) or problem(s) studiedAsthma and rhinitis
InterventionAllergy intervention - structured allergy history and skin prick testing and appropriate advice on allergy avoidance versus routine medical care
Intervention typeOther
Primary outcome measure(s)

1. Symptom scores (validated scale for asthma and rhinoconjunctivitis)
2. Health-related quality of life (using child or adult specific instruments)

Key secondary outcome measure(s)

1. Patients' subjective assessment of symptomatic improvement
2. Change in patient management (introduction or withdrawal of allergen avoidance)

Completion date01/05/2008

Eligibility

Participant type(s)Patient
Age groupAdult
SexAll
Target sample size at registration528
Key inclusion criteriaPatients with a working diagnosis of asthma and/or rhinoconjunctivitis
Key exclusion criteria1. Less than 5 years or greater than 50 years
2. Terminal illness
3. Confusional state
4. History of anaphylaxis
5. Tested in the preceding two years
Date of first enrolment01/05/2006
Date of final enrolment01/05/2008

Locations

Countries of recruitment

  • United Kingdom
  • England

Study participating centre

Brighton and Sussex Medical School
Brighton
BN1 9PH
United Kingdom

Results and Publications

Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
IPD sharing plan

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Results article results 01/03/2009 Yes No
Participant information sheet Participant information sheet 11/11/2025 11/11/2025 No Yes