跳至主要内容
临床试验/CTRI/2023/12/060861
CTRI/2023/12/060861招募中不适用

Mental Health Outcomes in Patients with Type 2 Diabetes Enrolled for the Diabetes Remission Study in India (DiRemI)

Freedom from diabetes research foundation (Host Institution)1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2024年1月1日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
300
试验地点
1
主要终点
Improvement in Mental Health outcomesAnxiety & Depression (in terms of reduction in

研究概览

简要总结

The proposed study is a single-arm pre-post design intervention trial that aims to assess the prevalence of depression, anxiety, and diabetes distress in patients with T2DM enrolled in a diabetes remission program and to determine the effect of the program in improving their mental health outcomes (anxiety, depression, and diabetes distress). Specific Objectives are: 1) To assess the prevalence of anxiety, depression, and diabetes distress in patients with T2D enrolled at the Freedom from Diabetes clinic for diabetes management through a lifestyle modification program. 2) To deliver an online intervention to improve mental health in those who have depression and anxiety. 3) To evaluate the effect of this intervention in reducing the prevalence of anxiety, depression, and diabetes distress scores among patients with T2D. 4) To study the effect of mental health on the outcome of the intervention in terms of remission and overall improvement in diabetes management. The intervention comprises lifestyle modification with a plant-based diet, exercise, psychological support, and medical management. Trained psychologists will provide a targeted intervention focusing on those with anxiety and depression through group therapy as well as individual counseling. The intervention will be 12 months (6-month intervention + 6-month follow-up). Data (socio-demographic data, administration of PHQ-9 scale, GAD-7, and T2-DDAS) will be collected at two-point times, at the baseline and end-line at the end of 6 months after the delivery of the intervention. Compliance data will be collected from patients based on their levels of both anxiety and depression. Adherence data will be collected from patients.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
30.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • Confirmed diagnosis of Type 2 Diabetes 2) Agree to examinations as per the study protocol, undergo the lifestyle intervention program & post-program evaluation 3)Participants who are well-oriented in time, and space & as a person 4)Provide written informed consent.

排除标准

  • Type 1 diabetes (due to autoimmune b-cell destruction, usually leading to absolute insulin deficiency, including latent autoimmune diabetes of adulthood).
  • Gestational Diabetes mellitus (diabetes diagnosed in the second or third trimester of pregnancy that was not clearly overt diabetes prior to gestation).
  • Specific types of diabetes due to other causes, eg., monogenic diabetes syndromes, diseases of exocrine pancreas, drug or chemical induced diabetes 4) Pregnant or lactating women 5) Patients who have required hospitalization for any diabetes-related complications in the last 6 months or for depression or are on antipsychotic drugs.

结局指标

主要结局

Improvement in Mental Health outcomesAnxiety & Depression (in terms of reduction in

时间窗: At baseline and at 6 months

scores below 10 for both anxiety & depression)

时间窗: At baseline and at 6 months

次要结局

  • 1) At least 10% reduction in weight and HbA1c(2) Improvement in co-morbidities and complications (nephropathy))

研究者

发起方
Freedom from diabetes research foundation (Host Institution)
申办方类型
Research institution
责任方
Principal Investigator
主要研究者

Dr Pramod Tripathi

Freedom from Diabetes Research Foundation

研究点 (1)

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