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Initial Specialist Telephone Consultation With New Patients in Secondary Care

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00988000
First Posted: October 1, 2009
Last Update Posted: June 8, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
The Dunhill Medical Trust
Information provided by (Responsible Party):
Imperial College London
  Purpose

Consultations with patients by hospital consultants are organised today in a manner which is barely dissimilar from that offered 30 or 40 years ago. Whilst some attempts to improve this process, such as Choose and Book, shorter waiting times and patients' receiving a copy of the correspondence sent to their general practitioner (GP) have improved the situation, there has been little radical change and little thought given to the patient experience.

The investigators wish to investigate whether patients' experience of attending respiratory outpatient clinics can be improved by a pre-clinic telephone call with a specialist thereby reducing the number of attendances at the hospital for appointments and investigations and improving overall patient satisfaction.


Condition Intervention
Respiratory Diseases Other: telephone consultation

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Health Services Research
Official Title: Telephone Consultations for New Patients Being Referred to a Specialist Respiratory Outpatient Clinic

Further study details as provided by Imperial College London:

Primary Outcome Measures:
  • Patient Satisfaction [ Time Frame: 2010 ]

Secondary Outcome Measures:
  • Patient costs [ Time Frame: 2010 ]
  • Patient views about outpatient experience [ Time Frame: 2010 ]
  • Reduction in number of required hospital attendances [ Time Frame: 2010 ]

Enrollment: 100
Study Start Date: June 2009
Study Completion Date: April 2010
Primary Completion Date: April 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Alternative appointment system
Alternative of telephone consultation (instead of face to face) offered as an initial consultation to new referrals
Other: telephone consultation
alternative to face to face consultation for new referrals

Detailed Description:

This study will investigate whether taking a new patient's history over the telephone permits better selection and arrangement of investigations prior to or synchronous with the first face to face consultation, with the potential to reduce the number of visits the patient has to make to the hospital.

Patients will be offered an initial telephone consultation by post and may opt-in or out of the study. Those having a telephone consultation would have this booked for a specific time and date and the patient would be sent an appropriate information leaflet regarding this. After the telephone consultation patients receive a summary of the consultation and details of any investigations and appointments booked by the research nurse. Patients who did not respond to the initial invitation letter within seven days or who declined to participate would be sent a routine appointment. All patients would asked to complete the MISS-21 questionnaire.

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • All new adult general respiratory referrals from primary care

Exclusion Criteria:

  • Follow-up patients
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00988000


Locations
United Kingdom
Imperial College at Charing Cross campus
London, United Kingdom, W6 8RF
Sponsors and Collaborators
Imperial College London
The Dunhill Medical Trust
Investigators
Principal Investigator: Professor MR Partridge, MD FRCP Imperial College London
  More Information

Responsible Party: Imperial College London
ClinicalTrials.gov Identifier: NCT00988000     History of Changes
Other Study ID Numbers: NHLICX07Q060519
First Submitted: September 30, 2009
First Posted: October 1, 2009
Last Update Posted: June 8, 2015
Last Verified: May 2010

Keywords provided by Imperial College London:
outpatients

Additional relevant MeSH terms:
Respiration Disorders
Respiratory Tract Diseases