Using Mobile Phone Short Message Service (SMS) Reminders to Enhance Appointment Attendance in DM Patients
1 other identifier
interventional
270
1 country
1
Brief Summary
A randomized controlled trial of patients with type 2 diabetes mellitus with multiple appointments into short message service group and control group. The attendance rate of these two groups of patients will be compared.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Nov 2016
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 2016
CompletedFirst Submitted
Initial submission to the registry
February 14, 2017
CompletedFirst Posted
Study publicly available on registry
February 16, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
March 30, 2018
CompletedFebruary 16, 2017
February 1, 2017
8 months
February 14, 2017
February 14, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Attendance Rate of the scheduled clinic appointment
Attendance Rate
between booking time and appointment time, usually within 1 weeks to 16 weeks
Study Arms (2)
SMS group
EXPERIMENTALreceive a mobile phone text reminder for scheduled clinic appointment 24-72 hours before,
Usual care group
NO INTERVENTIONUsual care, either telephone reminder or no reminder
Interventions
an SMS remind subjects to come for scheduled clinic appointment 24-72 hours before
Eligibility Criteria
You may qualify if:
- With diagnosis of type 2 diabetes
- Have more than 1 clinic services appointment under RAMP-DM programme:
- (e.g. blood taking, diabetic nurse individual counselling, group education, diabetic complication screening, retinal photo assessment, dietician counselling, etc)
You may not qualify if:
- Cannot read or receive appointment schedule on mobile phone
- Do not speak Cantonese/English or read Chinese/English
- Mentally incapacitated
- Pregnant Women
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- The University of Hong Konglead
- Hospital Authority, Hong Kongcollaborator
Study Sites (1)
Ha Kwai Chung General Outpatient Clinic
Kwai Chung, Hong Kong, 000, Hong Kong
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Man Chi Dao, M.B.B.S.
Resident
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 14, 2017
First Posted
February 16, 2017
Study Start
November 1, 2016
Primary Completion
June 30, 2017
Study Completion
March 30, 2018
Last Updated
February 16, 2017
Record last verified: 2017-02