Questionnaire Survey of Patients Using Accu-chek mobile

Questionnaire Survey of Patients Using Accu-chek mobile - QSACM

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000012088

Enrollment

Registered

2013-10-23

Start date

2013-08-01

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

diabetes mellitus

Interventions

SMBG machine and lancet device currently prescribed / Accu-chek mobile

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: patients with diabetes mellitus and receiving insulin or GLP-1 receptor agonist treatment under SMBG (self-monitoring of blood glucose)

Exclusion criteria

Exclusion criteria: patients who don&#39;t agree to this study

Design outcomes

Primary

Measure	Time frame
1) Evaluation on manipulation of SMBG devices (needle and monitor), 2) Impact on psychological and physical stress, comparing SMBG devices currently in use	—

Secondary

Measure	Time frame
1) Function of SMBG devices that would be found from the point of medical providers 2) Discrepancy of needs of patients and medical providers 3) Evaluation of Accu-chek mobile by medical providers 4) Possibility of lowering efforts by medical providers	—

Countries

Japan

Contacts

Public ContactMasafumi Matsuda

Saitama Medical Center, Saitama Medical University Depertment of Endocrinology and Diaebtes

matsudam-ind@umin.ac.jp+81-49-228-3564

Outcome results

None listed

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