跳至主要内容
临床试验/NCT07166016
NCT07166016招募中不适用

Evaluating the Effectiveness of Treatments on Gait Biomechanics in Patients With Hammertoe Deformities

University of Texas Rio Grande Valley2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年10月1日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
30
试验地点
2
主要终点
In-shoe Peak Plantar Pressure

研究概览

简要总结

This study looks at how hammertoe deformities affect foot pressure distribution and whether proper treatment can improve quality of life.

详细描述

Hammertoe deformities often lead to pain, discomfort, and difficulty with walking. People affected by these deformities are also at a higher risk for developing pressure-related ulcers on their feet. It is essential for clinicians to be aware of this risk and to assess the degree of plantar pressure reduction following both conservative and surgical treatments, as alleviating this pressure may help prevent the development of foot ulcers. Individuals diagnosed with hammertoes will participate in two data collection sessions-one visit before the intervention begins (pre-intervention) and another visit three months after the intervention (post-intervention).

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Confirmed distal symmetric sensory neuropathy.
  • MTPJ hyperextension deformity.
  • Claw or hammer toe deformity in toes.

排除标准

  • Non-hammertoe foot deformities affecting metatarsal head pressure.
  • Limited joint mobility, lower-limb amputation, or Charcot neuro-osteoarthropathy.
  • Peripheral vascular disease
  • Non-diabetic neuropathies
  • Significant lower-limb musculoskeletal issues
  • Rheumatoid arthritis
  • Current foot ulcer or edema
  • Inability to walk unaided
  • MRI contraindications
  • Morton's neuroma
  • History of foot surgery

结局指标

主要结局

In-shoe Peak Plantar Pressure

时间窗: Pre-intervention, Post-intervention (3 months)

In-shoe peak plantar pressure data will be recorded as patients walk with a pressure-measuring sensor placed inside their shoes. The unit will be Kilopascal (kPa).

次要结局

  • Quality of Life Questionnaire(Pre-intervention, Post-intervention (3 months))

研究者

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

Hafizur Rahman

Assistant Professor

University of Texas Rio Grande Valley

研究点 (2)

Loading locations...

相似试验