Trial Outcomes & Findings for Service Development: Assessing Non-attendance Rates in Outpatient Clinics (NCT NCT00129649)
NCT ID: NCT00129649
Last Updated: 2020-02-05
Results Overview
rates of attendance measured for scheduled clinics - attended patients
Recruitment status
COMPLETED
Study phase
NA
Target enrollment
504 participants
Primary outcome timeframe
after phone call within 1 week
Results posted on
2020-02-05
Participant Flow
Participant milestones
| Measure |
Control Group
This group received usual care and did not receive a telephone reminder
|
Telephone Reminder Group
This group received a telephone reminder for their clinic appointment
Telephone reminder call
|
|---|---|---|
|
Overall Study
STARTED
|
258
|
246
|
|
Overall Study
COMPLETED
|
182
|
181
|
|
Overall Study
NOT COMPLETED
|
76
|
65
|
Reasons for withdrawal
| Measure |
Control Group
This group received usual care and did not receive a telephone reminder
|
Telephone Reminder Group
This group received a telephone reminder for their clinic appointment
Telephone reminder call
|
|---|---|---|
|
Overall Study
Withdrawal by Subject
|
76
|
65
|
Baseline Characteristics
Service Development: Assessing Non-attendance Rates in Outpatient Clinics
Baseline characteristics by cohort
Baseline data not reported
PRIMARY outcome
Timeframe: after phone call within 1 weekPopulation: Lower participants number in the telephone reminder group, only participants who were could be contacted before the appointment
rates of attendance measured for scheduled clinics - attended patients
Outcome measures
| Measure |
Control Group
n=258 Participants
This group received usual care and did not receive a telephone reminder
|
Telephone Reminder Group
n=104 Participants
This group received a telephone reminder for their clinic appointment
Telephone reminder call
|
|---|---|---|
|
Attendance Rates at Respiratory Outpatient Clinics
|
183 Participants
|
89 Participants
|
Adverse Events
Control Group
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Telephone Reminder Group
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