Effectiveness of Holistic Lifestyle mHealth Intervention for Risk Reduction of Type 2 Diabetes Mellitus in Young Adults: A Randomized Controlled Trial
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 30
- 试验地点
- 1
研究概览
简要总结
The goal of this clinical trial (randomized controlled trial) is to examine the effectiveness of a holistic lifestyle mHealth intervention in reducing the risk of type 2 diabetes mellitus.
The study focuses on young adults aged 20-35 years, recruited from public and private universities in Rawalpindi and Islamabad, who meet the defined inclusion criteria.
The main questions it aims to answer are:
Does a holistic lifestyle mHealth intervention significantly reduce the risk of type 2 diabetes ? Does the intervention improve overall health-related quality of life and lifestyle behaviors, including diet, physical activity, and stress management?
详细描述
Researchers will compare participants receiving the holistic lifestyle mHealth intervention (based on "Eat Well, Move More, Stress Less") with a control group receiving standard care or basic health guidance to see if the intervention leads to greater reduction in diabetes risk and improved health outcomes.
Participants will:
Use a culturally tailored mHealth application designed for the Pakistani context Follow lifestyle recommendations focused on diet, physical activity, and stress management Engage with intervention content based on the three core pillars: Eat Well, Move More, Stress Less Participate in periodic assessments, including health measurements and questionnaires Provide feedback on their experience and adherence to the intervention
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Prevention
- 盲法
- None
入排标准
- 年龄范围
- 20 Years 至 35 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Young adults aged between 20-35 years, as defined by the WHO.
- •At risk of diabetes based on self-reported family history or lifestyle habits.
- •Participants who are willing to engage in the mHealth intervention program.
- •Own a smartphone and are familiar with using mobile apps.
- •Complete the informed consent process, agreeing to follow the study protocol, including survey completion and health assessment.
排除标准
- •Individuals diagnosed with chronic mental or physical illnesses
- •Individuals with hearing or vision loss so severe that they could not access the mobile health intervention.
- •Pregnant women or women who plan on becoming pregnant during the study.
- •Individuals who are already taking part in an equivalent diabetes or health programme.
- •Individuals who are not willing to provide consent.
研究者
Anmol Ayaz
Principal Investigator
Fatima Jinnah Women University