Method to encourage consultation for people in Impaired Glucose Tolerance: a randomized control trial

Method to encourage consultation for people in Impaired Glucose Tolerance: a randomized control trial - to go see doc trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000035069

Enrollment

490

Registered

2019-02-01

Start date

2019-05-17

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Impaired Glucose Tolerance

Interventions

Intervention: new method of explanation Control: conventional method of explanation

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: (1) 20-75y-o at the point of the comprehensive medical check. (2) Correspond one of followings. a) HbA1c: 6.0-6.4% b) Fasting blood sugar: 110-125 mg/dL c) Blood sugar after two hours of oral glucose tolerance test: 140-199 mg/dL

Exclusion criteria

Exclusion criteria: (1) Undergoing treatment of Diabetes mellitus at the point of the comprehensive medical check. (2) Not be proved the results of the comprehensive medical check in the test day. (3) Need informed assent. (4) Not agree with participating in the study.

Design outcomes

Primary

Measure	Time frame
A rate of people who go for medical consultation related to Impaired Glucose Tolerance.	—

Secondary

Measure	Time frame
(1) A rate of people who get worse of their Impaired Glucose Tolerance. (2) Changing in blood sugar. (3) Changing in HbA1c.	—

Countries

Japan

Contacts

Public ContactManako Konda

Kyoto University School of Public Health Department of Preventive Services

konda.manako.53v@st.kyoto-u.ac.jp075-753-2431

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026