Tokyo, July 14 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000062158) titled 'Evaluation of Patient-Participatory Multidisciplinary Conferences in Diabetes Care' on July 14.
Study Type:
Interventional
Study Design:
Basic Design - Parallel
Randomization - Randomized
Blinding - Open -no one is blinded
Control - Active
Primary Sponsor:
Institute - Gunma University
Condition:
Condition - Diabetes
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - To evaluate the effects of patient-participatory multidisciplinary conferences compared with conventional conferences on glycemic control, clinical parameters, patient-reported outcomes, healthcare professional assessments, and qualitative outcomes in patients admitted for diabetes education.
Basic objectives2 - Efficacy
Intervention:
Interventions/Control_1 - Patient-participatory multidisciplinary conferences will be conducted for hospitalized patients with diabetes. Patients will participate in multidisciplinary conferences together with healthcare professionals, including physicians, nurses, registered dietitians, and pharmacists, to share information and discuss their medical condition, self-management issues, and treatment plans.
Interventions/Control_2 - Conventional multidisciplinary conferences will be conducted for hospitalized patients with diabetes. Healthcare professionals, including physicians, nurses, registered dietitians, and pharmacists, will discuss the patient's medical condition, self-management issues, and treatment plans without patient participation.
Eligibility:
Age-lower limit - 18
years-old
<=
Age-upper limit - Not applicable
Gender - Male and Female
Key inclusion criteria - [Patients]
1)Patients aged 18 years or older
2)Patients with diabetes
3)Hospitalized patients
4)Patients who provide written informed consent to participate in the study
[Healthcare professionals]
1)Healthcare professionals involved in the diagnosis, care support, or treatment planning of eligible patients and participating in the study conferences
2)Healthcare professionals who provide written informed consent to participate in the study
Key exclusion criteria - [Patients]
1)Patients with severe visual impairment due to diabetic retinopathy or other causes.
2)Patients diagnosed with dementia.
3) Patients judged to be unsuitable for participation by a physician.
[Healthcare professionals]
1)Healthcare professionals unable to complete the questionnaire or participate in the interview.
2) Healthcare professionals judged to be unsuitable for participation by a physician.
Target Size - 130
Recruitment Status:
Recruitment status - Preinitiation
Date of protocol fixation - 2026 Year 04 Month 28 Day
Date of IRB - 2026 Year 06 Month 01 Day
Anticipated trial start date - 2026 Year 07 Month 14 Day
Last follow-up date - 2028 Year 03 Month 31 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000071131
Disclaimer: Curated by HT Syndication.
