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Initial Specialist Telephone Consultation With New Patients in Secondary Care

Telephone Consultations for New Patients Being Referred to a Specialist Respiratory Outpatient Clinic

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00988000
Enrollment
157
Registered
2009-10-01
Start date
2009-06-30
Completion date
2010-04-30
Last updated
2019-10-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Respiratory Diseases

Keywords

outpatients

Brief summary

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.

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.

Interventions

alternative to face to face consultation for new referrals

OTHERNo intervention

no alternative to face to face consultation

Sponsors

The Dunhill Medical Trust
CollaboratorOTHER
Imperial College London
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All new adult general respiratory referrals from primary care

Exclusion criteria

* Follow-up patients

Design outcomes

Primary

MeasureTime frameDescription
Patient Satisfaction of the Alternative ConsultationFirst clinic appointment (Month 0) and Follow-up appointment (6 monthsPatient Satisfaction assessed by MISS scale, Medical interview satisfaction score. The score 0-7, 0 means dissatisfaction, higher scores indicate higher satisfaction.

Secondary

MeasureTime frameDescription
Number of Required Investigations0-6 monthsreduction in number of required investigations

Countries

United Kingdom

Participant flow

Pre-assignment details

Patients' who attending respiratory outpatient clinics

Participants by arm

ArmCount
Respond to Study Invitation - Agree to Alternative Consultatio
participants agreed to have an alternative consultation i.e. telephone consultation for their first hospital appointment
49
Respond to Study Invitation - Declined/ Non-responders
Participants declined or did not respond to the invitation to participate in the study
51
Comparator - Choose and Book
participants in this group booked their appointment through the choose and book system
57
Total157

Baseline characteristics

CharacteristicRespond to Study Invitation - Declined/ Non-respondersComparator - Choose and BookTotalRespond to Study Invitation - Agree to Alternative Consultatio
Age, Continuous57.4 years
STANDARD_DEVIATION 16.7
50.9 years
STANDARD_DEVIATION 17
56.7 years
STANDARD_DEVIATION 15.8
62 years
STANDARD_DEVIATION 13.7
Race and Ethnicity Not Collected0 Participants
Region of Enrollment
United Kingdom
51 participants57 participants157 participants49 participants
Sex: Female, Male
Female
28 Participants28 Participants83 Participants27 Participants
Sex: Female, Male
Male
23 Participants29 Participants74 Participants22 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
deaths
Total, all-cause mortality
0 / 490 / 510 / 57
other
Total, other adverse events
0 / 490 / 510 / 57
serious
Total, serious adverse events
0 / 490 / 510 / 57

Outcome results

Primary

Patient Satisfaction of the Alternative Consultation

Patient Satisfaction assessed by MISS scale, Medical interview satisfaction score. The score 0-7, 0 means dissatisfaction, higher scores indicate higher satisfaction.

Time frame: First clinic appointment (Month 0) and Follow-up appointment (6 months

Population: Incomplete data and those that had an alternative consultation did not need a follow up appointment

ArmMeasureGroupValue (MEAN)Dispersion
Agree to the Alternative ConsultationPatient Satisfaction of the Alternative Consultationfirst clinic appointment5.85 score on a scaleStandard Deviation 0.73
Declined the Alternative Study InvitationPatient Satisfaction of the Alternative Consultationfirst clinic appointment5.67 score on a scaleStandard Deviation 0.68
Declined the Alternative Study InvitationPatient Satisfaction of the Alternative Consultationfollow-up appointment5.47 score on a scaleStandard Deviation 0.53
ComparatorPatient Satisfaction of the Alternative Consultationfirst clinic appointment5.26 score on a scaleStandard Deviation 0.7
ComparatorPatient Satisfaction of the Alternative Consultationfollow-up appointment5.36 score on a scaleStandard Deviation 0.98
Secondary

Number of Required Investigations

reduction in number of required investigations

Time frame: 0-6 months

ArmMeasureGroupValue (NUMBER)
Agree to the Alternative ConsultationNumber of Required InvestigationsPlanned investigations147 number of investigation
Agree to the Alternative ConsultationNumber of Required InvestigationsCompleted investigations145 number of investigation
Declined the Alternative Study InvitationNumber of Required InvestigationsPlanned investigations117 number of investigation
Declined the Alternative Study InvitationNumber of Required InvestigationsCompleted investigations105 number of investigation
ComparatorNumber of Required InvestigationsPlanned investigations128 number of investigation
ComparatorNumber of Required InvestigationsCompleted investigations116 number of investigation

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026