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临床试验/NCT06402578
NCT06402578尚未招募不适用

A Feasibility Randomised Controlled Trial to Investigate the Effects of a 12-week Digital Physical Activity Programme, With or Without Physical Education Support, on Blood Glucose Control in Patients With Type 2 Diabetes Mellitus

Queen Margaret University2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年6月最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
60
试验地点
2
主要终点
HbA1c testing

研究概览

简要总结

Investigation into the effects of a 12-week digital physical activity programme, with or without physical education support on blood glucose control in patients with T2DM using HbA1c testing.

详细描述

Primary objective: investigate the effects of a 12-week digital physical activity programme, with or without physical education support on blood glucose control in patients with T2DM using HbA1c testing. Secondary objective: evaluate the effects on Cholesterol (ratio of High Density Lipids to Low Density Lipids), Resting Heart Rate, and Body Mass Index after a 12 week physical activity programme. Monitor step counts and sleep patterns during a 12 week physical activity programme.: Methods: Using a RCT is intended to implement dependent variable inductive research into a 12-week e-Health Physical activity (PA) programme with or without physical education support focusing on the blood glucose control in patients with T2DM. Recruitment of 60 patients from hospital out-patient clinics, community diabetic departments, and. NHS patients from general practitioners.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • A diagnosis of T2DM in the last 3 years.
  • Age 18+ years.
  • Uses the English language as a primary or secondary language with the ability to read and write.
  • Lives in the United Kingdom.
  • Has no medical reason preventing participation in regular physical activity.
  • Has a SMART phone with access to the internet.

排除标准

  • Physical inability to participate in 12 weeks of physical activity.
  • Cardiac or cardiovascular surgery in the past 6 months.
  • Musculoskeletal issues that could be aggravated whilst participating in regular physical activity.
  • Presently participating in a weight loss programme.
  • Unable to commit to the 12-week feasibility study.

结局指标

主要结局

HbA1c testing

时间窗: 12 weeks

blood will be take pre and post trial.

次要结局

  • Cholesterol ratio testing(12 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Phil Calvert

Principal Investigator

Queen Margaret University

研究点 (2)

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