ClinicalTrials.gg
RecruitingNCT06176703Updated Dec 29, 2023

Mobile Application for Self-Management of Type 2 Diabetes Mellitus

An interventional study of mobile application in Diabetes Mellitus, Type 2, sponsored by Ramathibodi Hospital. Recruiting at 1 site in Thailand. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-12-29.

Sponsored by Ramathibodi Hospital · Not applicable, Interventional, and Health services research

From the registry’s dates

  • Primary completion was expected by Jun 2025, 1 year 4 months ago, but the record still lists the study as recruiting.
  • Started Nov 2023; still recruiting 2 years 11 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
128
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this Randomized Controlled Trial is to study the effect of mobile Application on glycemic control of type2 diabetes mellitus. The main questions aim to answer are:

  • The effect of mobile application on glycemic control and quality of life of diabetes mellitus patients
  • The satisfaction of mobile application of diabetes mellitus patients who used it Participants will be received education about diabetes mellitus and separated into two groups, intervention group(using mobile application) and control group(not using mobile application but also receive standard treatment of diabetes mellitus.

Researchers will compare intervention group to control group about glycemic control including HbA1c, complications of diabetes mellitus etc. and quality of life.

02

Conditions studied

  • Diabetes Mellitus, Type 2
03

In context

Diabetes Mellitus, Type 2

10,371 studies on the registry are indexed under Diabetes Mellitus, Type 2; 1,406 are open to participants now.

This study's planned enrollment of 128 is above the median of 80 across 8,350 interventional studies indexed under Diabetes Mellitus, Type 2.

Browse Diabetes Mellitus, Type 2 studies →

Lead sponsor

Ramathibodi Hospital is the lead sponsor of 63 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Type2 diabetes mellitus who have above 7%
  • Can use application on smartphone
  • age 18 years old or more (relatives are accept if participants have age more than 65 years old and cannot use smartphone)
  • consent to participate the research

Exclusion criteria

Exclusion Criteria:

  • refuse to participate the research
  • pregnancy
  • using continuous glucose monitoring system or insulin pump
  • disability in sight or hearing
  • have been using the mobile application(RAMAdiabetes) in the past
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

HbA1c

A blood test of average blood sugar over the past two to three months, given as a percentage or in mmol/mol. 6.5% (48 mmol/mol) or more is the usual threshold for diabetes, normally confirmed by a second test.

05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Care provider, Outcomes assessor)
Enrollment
128 participants (estimated)

Study arms

  • Experimental
    Standard treatment with mobile application in diabetes mellitus patients

    Device: mobile application

  • No intervention
    standard treatment without mobile application in diabetes mellitus patients

Interventions

  • Devicemobile application

    using mobile application along with standard treatment of diabetes mellitus

06

What researchers measure

Primary outcomes

  1. Glycemic control

    HbA1c

    Time frame: 3-6 months

  2. Glycemic control

    Fasting blood sugar

    Time frame: 3-6 months

Secondary outcomes

  1. self-diabetes management

    The Thai-Diabetes Management of Self-Efficacy Scale(T-DMSES), total score range from 19 to 95 points(minimum to maximum), each question has 1 to 5 points, higher scores mean better self diabetes management

    Time frame: 3-6 months

  2. Quality of life

    The Thai version of the EQ-5D-5L Health Questionnaire

    Time frame: 3-6 months

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Nov 2023 (actual). Primary completion is estimated for Jun 2025, 19 months after the start.

Of 2,066 non-industry interventional studies with no phase under Diabetes Mellitus, Type 2, half reached primary completion within 21 months of starting (the median), counting those still running; a quarter within 10 and three quarters within 40. This study's planned 19 months is close to that.

Counting every sponsor, half of 2,243 studies reached it within 21 months; a quarter within 10 and three quarters within 39.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 5, 2023
First posted
Dec 20, 2023
StartActual
Nov 22, 2023
Primary completionEst.
Jun 30, 2025
CompletionEst.
Nov 22, 2025
Last update
Dec 29, 2023
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Dec 29, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06176703
Lead sponsor
Ramathibodi Hospital
Responsible party
Supasuta Wongdama (Principal Investigator, Ramathibodi Hospital) — Principal investigator
First posted
Dec 20, 2023
Start date
Nov 22, 2023
Primary completion
Jun 30, 2025 (estimated)
Completion
Nov 22, 2025 (estimated)
Last update
Dec 29, 2023

Study contacts

Supasuta Wongdama, Fellowship
Contact
poytriplet@gmail.com
0905754190
Chutintorn Sriphrapradang
study director · Ramathibodi Hospital

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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