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. 2002 Jul 22;2002(3):CD001117. doi: 10.1002/14651858.CD001117

Cote 1997.

Methods DESIGN: Randomised controlled trial of two interventions 
 METHOD OF RANDOMISATION: Randomised ‐ stratified randomisation 
 MEANS OF ALLOCATION CONCEALMENT‐ not stated. 
 OUTCOME ASSESSOR BLINDING ‐ not blinded. 
 WITHDRAWAL/DROPOUTS ‐ all subjects accounted for.
Participants Eligible: not specified 
 Randomised: 188 (Peak Flow 62, Symptoms Only 52, Control 74) 
 Completed: 149 (Peak Flow 50, Symptoms Only 45, Control 54) 
 Age: Overall mean: 36 yrs Range: 
 Sex: Male/Female ‐ 
 Asthma Diagnosis: Doctor's diagnosis and objective lung function 
 Recruitment: Hospital admissions or visit to a clinic. 
 Diseases Included: 
 Major exclusions: current and ex‐smokers 40 yr of age or older in whom the best FEV1 after salbutamol was < 80% of predicted, patients with significant concurrent diseases, those requiring > 7.5 mg prednisone to control asthma symptoms and those who had already taken part in an asthma education program. 
 Baseline: 
 FEV1: not stated 
 PEF: % predicted: Peak Flow 93+/‐3; Symptoms 91+/‐3; Control 95+/‐3. 
 Exacerbations not stated
Interventions Setting: tertiary care setting 
 Type: Two optimal interventions and an active control. 
 (1) Education, peak flow self monitoring, regular review and individualised written action plan based on peak flow enabling self adjustment of medications in the event of worsening asthma. 
 (2) Education, symptoms self monitoring, regular review and a symptoms based written action plan enabling self adjustment of medications in the event of worsening asthma. 
 (3) Control group: Taught inhaler technique by the educator and about medication use and triggers by their pulmonologist. Their physician may have provided a verbal action plan. 
 Duration: A minimum of 1 x one hour one to one counselling sessions for both educated groups
Outcomes Knowledge, compliance, hospitalisations, ER visits, oral corticosteroids, days lost from work or school.
Notes Jadad Score = 4
Treatment was optimised for all subjects during baseline.
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? Unclear risk Information not available (Cochrane Grade B)