Integrated Care and Counseling for Frail Older Patients with Diabetes
Effectiveness of Integrated Care Combined Nutrition and Lifestyle Counselling in Frail Older Patients With Diabetes
Recruiting
N/AInterventional Study
FrailtyDiabetesLifestyle
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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Review the details below, then apply to join this clinical trial.
At a Glance
Age
65 and older
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
100 (estimated)
Sponsor
Buddhist Tzu Chi General Hospital · Other
Who this trial is looking for
This trial is looking for older adults with frailty and diabetes. Participants will receive 12 weeks of support that includes health education and personalized guidance on nutrition and lifestyle.
Are You a Good Fit for This Trial?
You may be able to join if
I am 65 years or older.
I have a Clinical Frailty Scale score between 4 and 7.
I have been diagnosed with type 2 diabetes or my HbA1c is 6.5% or higher.
I can understand the research process and provide consent.
You may not be able to join if
I am unable to cooperate with the study or participate in follow-up.
I have a history of type 1 diabetes.
I use insulin injections or pumps.
I have a serious medical condition that is poorly controlled.
I have severe visual or hearing impairments.
I have been diagnosed with a malignant tumor recently or am undergoing treatment.
I have received hormone therapy within the last three months.
I am currently in any other physical training courses or nutrition plans.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
The goal of this clinical trial is to evaluate the effectiveness of innovative integrated care in pre-frail or frail patients with diabetes over 65 years old. The main questions it aims to answer are:
* To establish innovative integrated care for frail elderly patients with diabetes combined with nutrition and lifestyle guidance.
* To evaluate the effectiveness of the intervention compared with g…
The goal of this clinical trial is to evaluate the effectiveness of innovative integrated care in pre-frail or frail patients with diabetes over 65 years old. The main questions it aims to answer are:
* To establish innovative integrated care for frail elderly patients with diabetes combined with nutrition and lifestyle guidance.
* To evaluate the effectiveness of the intervention compared with general outpatient care.
Participants will receive 12 weeks of structured care including specialist care, integrated assessment, group health education, one-on-one nutrition and lifestyle guidance, online and face-to-face support group, and case management. Researchers will compare general outpatient care to see its effects on frailty, physical function, and blood sugar control.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* People aged 65 years or older.
* People with Clinical Frailty Scale: 4-7.
* People with a history of type II diabetes, use of diabetes medications, or HbA1c greater than or equal to 6.5%.
* People can understand the research process, meet the requirements of the research, and …
Inclusion Criteria:
* People aged 65 years or older.
* People with Clinical Frailty Scale: 4-7.
* People with a history of type II diabetes, use of diabetes medications, or HbA1c greater than or equal to 6.5%.
* People can understand the research process, meet the requirements of the research, and can sign the informed consent and participate in the following tracking.
Exclusion Criteria:
* People that are unable to cooperate with or accept intervention or follow-up.
* People with a history of type I diabetes.
* People use insulin injections or pumps.
* According to the PI's judgment, people with severe or poorly controlled conditions include acute diseases, severe infections, severe abnormal laboratory tests, or serious medical conditions with the following systems: cardiovascular, pulmonary, hepatic, nervous, mental, metabolic, renal, musculoskeletal, gastrointestinal, etc.
* People with severe visual or hearing impairment that prevent the completion of assessment and testing.
* People with malignant tumors that have just been diagnosed or are undergoing treatment or are still at risk of recurrence.
* People have received hormone therapy within three months before the trial or are expected to receive hormone therapy during the trial.
* People are currently or expected to join any other physical training courses or nutrition plans during the trial.
* Others are based on the judgment of the PI that participating in this trial may adversely affect the safety of the subjects, hinder the progress of the experiment, or interfere with the evaluation of the outcomes of the trial.
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