跳至主要内容
临床试验/CTRI/2024/05/066755
CTRI/2024/05/066755已完成3 期

Effect of blood flow restriction training on foot pain, disability and functional activities of daily living among diabetic adult population- A randomized controlled trial

Galgotias University1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2024年5月15日最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
50
试验地点
1
主要终点
Foot function Index will be used to assess foot-related pain, disability, and activity limitations

研究概览

简要总结

This randomized controlled trial investigates the impact of blood flow restriction training on foot pain, disability, and functional activities of daily living in diabetic adults. Participants will be randomized into intervention and control groups, with the intervention group undergoing blood flow restriction training while the control group receives standard care. Outcome measures include foot pain intensity, disability using the Foot Function Index, and functional activities of daily living using the SF-36 Health Survey. The study aims to provide insights into the efficacy of blood flow restriction training in improving the quality of life and functional outcomes in diabetic individuals with foot complications.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
20.00 Year(s) 至 50.00 Year(s)(—)
性别
All

入选标准

  • Diabetic adults (Type 1 or Type 2).
  • Presence of foot pain, disability, or limitations in daily activities.
  • Stable medical condition without contraindications for exercise.

排除标准

  • Severe peripheral vascular disease.
  • Recent foot ulcerations or infections.
  • Inability to participate in exercise programs due to other medical conditions.

结局指标

主要结局

Foot function Index will be used to assess foot-related pain, disability, and activity limitations

时间窗: Baseline, 4 weeks and after 6 weeks.

The Barthel Index Wwill be used for assessing activities of daily living (ADL)

时间窗: Baseline, 4 weeks and after 6 weeks.

次要结局

  • SF36 The SF-36 will be used to assess health-related quality of life(Baseline, 4 weeks and 6 weeks)

研究者

发起方
Galgotias University
申办方类型
Research institution
责任方
Principal Investigator
主要研究者

Dr Adarsh Kumar Singh

Galgotias University

研究点 (1)

Loading locations...

相似试验