Trial Outcomes & Findings for Initial Specialist Telephone Consultation With New Patients in Secondary Care (NCT NCT00988000)
NCT ID: NCT00988000
Last Updated: 2019-10-25
Results Overview
Patient Satisfaction assessed by MISS scale, Medical interview satisfaction score. The score 0-7, 0 means dissatisfaction, higher scores indicate higher satisfaction.
Recruitment status
COMPLETED
Study phase
NA
Target enrollment
157 participants
Primary outcome timeframe
First clinic appointment (Month 0) and Follow-up appointment (6 months
Results posted on
2019-10-25
Participant Flow
Patients' who attending respiratory outpatient clinics
Participant milestones
| Measure |
Agree to Alternative Study Invitation
Patients Respond to study invitation - agree to alternative consultation
|
Declined the Alternative Study Invitation
Patients respond to study invitation - declined/ non-responders for the invitation
|
Comparator
Patients - choose and book
|
|---|---|---|---|
|
Overall Study
STARTED
|
49
|
51
|
57
|
|
Overall Study
COMPLETED
|
49
|
51
|
57
|
|
Overall Study
NOT COMPLETED
|
0
|
0
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Race and Ethnicity were not collected from any participant.
Baseline characteristics by cohort
| Measure |
Respond to Study Invitation - Agree to Alternative Consultatio
n=49 Participants
participants agreed to have an alternative consultation i.e. telephone consultation for their first hospital appointment
|
Respond to Study Invitation - Declined/ Non-responders
n=51 Participants
Participants declined or did not respond to the invitation to participate in the study
|
Comparator - Choose and Book
n=57 Participants
participants in this group booked their appointment through the choose and book system
|
Total
n=157 Participants
Total of all reporting groups
|
|---|---|---|---|---|
|
Sex: Female, Male
Male
|
22 Participants
n=49 Participants
|
23 Participants
n=51 Participants
|
29 Participants
n=57 Participants
|
74 Participants
n=157 Participants
|
|
Race and Ethnicity Not Collected
|
—
|
—
|
—
|
0 Participants
Race and Ethnicity were not collected from any participant.
|
|
Region of Enrollment
United Kingdom
|
49 participants
n=49 Participants
|
51 participants
n=51 Participants
|
57 participants
n=57 Participants
|
157 participants
n=157 Participants
|
|
Age, Continuous
|
62 years
STANDARD_DEVIATION 13.7 • n=49 Participants
|
57.4 years
STANDARD_DEVIATION 16.7 • n=51 Participants
|
50.9 years
STANDARD_DEVIATION 17.0 • n=57 Participants
|
56.7 years
STANDARD_DEVIATION 15.8 • n=157 Participants
|
|
Sex: Female, Male
Female
|
27 Participants
n=49 Participants
|
28 Participants
n=51 Participants
|
28 Participants
n=57 Participants
|
83 Participants
n=157 Participants
|
PRIMARY outcome
Timeframe: First clinic appointment (Month 0) and Follow-up appointment (6 monthsPopulation: Incomplete data and those that had an alternative consultation did not need a follow up appointment
Patient Satisfaction assessed by MISS scale, Medical interview satisfaction score. The score 0-7, 0 means dissatisfaction, higher scores indicate higher satisfaction.
Outcome measures
| Measure |
Agree to the Alternative Consultation
n=44 Participants
Patients respond to study invitation and agree
|
Declined the Alternative Study Invitation
n=29 Participants
Declined/non-responders for the invitation
|
Comparator
n=41 Participants
Patients choose and book
|
|---|---|---|---|
|
Patient Satisfaction of the Alternative Consultation
first clinic appointment
|
5.85 score on a scale
Standard Deviation 0.73
|
5.67 score on a scale
Standard Deviation 0.68
|
5.26 score on a scale
Standard Deviation 0.70
|
|
Patient Satisfaction of the Alternative Consultation
follow-up appointment
|
—
|
5.47 score on a scale
Standard Deviation 0.53
|
5.36 score on a scale
Standard Deviation 0.98
|
SECONDARY outcome
Timeframe: 0-6 monthsreduction in number of required investigations
Outcome measures
| Measure |
Agree to the Alternative Consultation
n=49 Participants
Patients respond to study invitation and agree
|
Declined the Alternative Study Invitation
n=51 Participants
Declined/non-responders for the invitation
|
Comparator
n=57 Participants
Patients choose and book
|
|---|---|---|---|
|
Number of Required Investigations
Planned investigations
|
147 number of investigation
|
117 number of investigation
|
128 number of investigation
|
|
Number of Required Investigations
Completed investigations
|
145 number of investigation
|
105 number of investigation
|
116 number of investigation
|
Adverse Events
Agree to Alternative Study Invitation
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Declined the Alternative Study Invitation
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Comparator
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place