跳至主要内容
临床试验/NCT01914991
NCT01914991已完成4 期

Treatment of the PIP Joint Flexion Contracture: Combined Static and Dynamic Orthotic Intervention Compared With Traditional Combine Therapy. A Randomized Controlled Trial

University of Malaga2 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2011年6月最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
62
试验地点
2
主要终点
Active Range of motion AROM (degrees)

研究概览

简要总结

Study Design: Randomized controlled clinical study. Introduction: Physiotherapeutic intervention aiming to restore mobility using different techniques as stretching, hot packs, exercises, therapeutic ultrasound and orthotics. No scientific evidence has been found correlating improved joint mobility and the use of these techniques. Application techniques of orthoses to reshape the soft tissues have been well detailed, however, no scientific evidence supporting their effectiveness on proximal interphalangeal joint (PIPJ) lag extension resolution using them as a single treatment has been found.

Purpose of the Study: The purpose of the study was to test the effectiveness of static and dynamic orthosis in patients with a PIPJ flexion retraction using them as a single treatment compared with traditional combined therapies.

Method: 63 participants were included in the study. Patients who used splints were compared to a control group who received conventional treatment. Active and passive mobility were measured before the experiment and again three months after. All the patients were measured under the same conditions and treated by the same hand therapist. The relationship between contracture resolution and function was measured using the DASH Spanish Version.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Active Range of motion AROM (degrees)

时间窗: baseline; post-treatment (3 moths)

AROM and function were measured in all patients at inclusion and at three months after the start of the study. which was measured using a short arm goniometer Stainless Baseline 180°. A lateral measurement following the standardized protocol recommended by the American Society of Hand Therapists was used.

次要结局

  • Disability of the arm shoulder AND HAND (DASH QUESTIONNAIRE)(baseline; post-treatment (3 moths); 24 weeks follow up)
  • changes from postreatment Active range of Motion (AROM) degrees(24 weeks follow up)

研究者

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

Dr. Antonio I Cuesta-Vargas

PhD

University of Malaga

研究点 (2)

Loading locations...

相似试验