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Clinical Trials/NCT00129649
NCT00129649
Completed
Not Applicable

Service Development: Assessing Non-attendance Rates in Outpatient Clinics

Imperial College London1 site in 1 country504 target enrollmentOctober 2005

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Asthma
Sponsor
Imperial College London
Enrollment
504
Locations
1
Primary Endpoint
Attendance Rates at Respiratory Outpatient Clinics
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Many studies have shown a high non-attendance rate in hospital outpatient clinics. The investigators have found a non-attendance rate of 25% in their asthma clinics and would like to investigate whether a reminder phone call will improve attendance rates. Patients will be randomised into two groups; one group will receive a reminder phone call one week prior to their hospital consultation and the other group will be managed in the standard manner (i.e. no reminder of any sort). The phone calls will be carried out on a Friday afternoon by a respiratory nurse specialist and a research officer for two asthma clinics based on a Wednesday morning and a Thursday afternoon.

Detailed Description

Many studies have shown a high non-attendance rate in hospital outpatient clinics. The investigators have found a non-attendance rate of 25% in their asthma clinics and would like to investigate whether a reminder phone call will improve attendance rates. Patients will be randomised into two groups; one group will receive a reminder phone call one week prior to their hospital consultation and the other group will be managed in the standard manner (i.e. no reminder of any sort). The phone calls will be carried out on a Friday afternoon by a respiratory nurse specialist and a research officer for two asthma clinics based on a Wednesday morning and a Thursday afternoon. To have an 80% chance of detecting a 10% reduction in non-attendance rates (at 5%) 500 patients are required for this study. The rate of non-attendance will be monitored for all the patients in both groups and some demographic information will be recorded for each patient(age, sex, diagnosis and home postcode).

Registry
clinicaltrials.gov
Start Date
October 2005
End Date
November 2006
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with appointments booked for 2 respiratory outpatient clinics
  • Exclusion criteria
  • Patients likely to only need one appointment

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Attendance Rates at Respiratory Outpatient Clinics

Time Frame: after phone call within 1 week

rates of attendance measured for scheduled clinics - attended patients

Study Sites (1)

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