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临床试验/NCT06272877
NCT06272877已完成不适用

Effectiveness of Fluidotherapy in Patients With Conservatively Treated Distal Radius Fractures

Ahi Evran University Education and Research Hospital2 个研究点 分布在 2 个国家目标入组 40 人开始时间: 2024年3月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
40
试验地点
2
主要终点
Visual analog scale

研究概览

简要总结

Distal radius fractures are the most common fractures when looking at upper extremity fractures. The incidence of distal radius fractures is increasing day by day, and when looking at the databases of various countries, its annual prevalence reaches 70,000 in the UK and 640,000 in the USA. Most of these fractures are related to osteoporosis and require appropriate treatment. If not, it causes loss of work force, permanent disability, and limitation in daily activities.

Fluidotherapy has also proven to be effective in reducing hand edema in patients with carpal tunnel syndrome and stroke, examining its effect on nerve conduction velocities, and warming hypothermic patients. Compared to these treatment methods, fluid therapy reduces both joint capsule and muscle temperature by 9°C and 5.7°C, respectively. has been reported to increase.

详细描述

Reducing pain and edema after Distal Radius fracture is an important part of postoperative rehabilitation. Various massage and mobilization methods were applied to this patient population in the postoperative period. In a recent study evaluating the effectiveness of Whirlpool treatment, it was reported that studies on the effectiveness of fluidotherapy are also needed. There is no study in the literature evaluating the effectiveness of fluidotherapy in the postoperative rehabilitation program in patients who underwent surgery for distal radius fractures.

This study aimed to evaluate the effect of adding fluidotherapy to the early rehabilitation program on pain, edema, joint range of motion and functionality after the cast is removed in patients who received conservative cast treatment due to distal radius fracture.

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
Double (Investigator, Outcomes Assessor)

盲法说明

The Investigator and the outcomes assesor will be different persons. Statician will be different person.

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Treating with a cast due to distal radius fracture being over 18 years old

排除标准

  • Presence of polytrauma
  • History of previous limb-related surgery
  • Hemiplegia in the involved limb
  • Contracture in the involved limb
  • Arterial and venous occlusions
  • Lymphatic system disorders
  • Heart and circulatory system disorders
  • Hepatitis, Measles, Sepsis infectious diseases or fever
  • Open wound on the applied hand.

研究组 & 干预措施

Fluidotherapy Group

Experimental

Fluidotherapy will be applied to the group in addition to the conservative rehabilitation program received by the control group. Fluidotherapy will be applied 20 minutes a day, 5 days a week for 4 weeks.

干预措施: Fluidotherapy (Other)

Fluidotherapy Group

Experimental

Fluidotherapy will be applied to the group in addition to the conservative rehabilitation program received by the control group. Fluidotherapy will be applied 20 minutes a day, 5 days a week for 4 weeks.

干预措施: conventional rehabilitation program (Other)

Control group

Active Comparator

Only the conventional rehabilitation program will be applied by a physiotherapist for 6 weeks.

干预措施: conventional rehabilitation program (Other)

结局指标

主要结局

Visual analog scale

时间窗: 6th week

Visual analog scale (VAS) was used for pain assessment. VAS is a 10-point Likert scale.A score of 0 indicates the best result, a score of 10 indicates the worst result. Higher scores indicate higher pain.

Wrist joint range of motion

时间窗: 6th week

Wrist joint range of motion: Measurement of wrist joint range of motion (ROM) with a goniometer is the most frequently used method in clinical practice that provides objective evaluation and error-free measurement. In our study, wrist ROM measurements will be made with a goniometer using the neutral zero method. This method is a painless and non-invasive measurement method.

Circumference (mm)

时间窗: 6th week

Environmental Measurement; the both hands and wrists of the patient will be measured with the help of a tape measure using the figure of eight method. The cm difference between both upper extremities will be recorded.

次要结局

  • Gross Grip Strength:(6th week)
  • Patient-Rated Wrist Evaluation (PRWE) questionnaire(6th week)

研究者

发起方
Ahi Evran University Education and Research Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Levent Horoz

Principal Investigator

Ahi Evran University Education and Research Hospital

研究点 (2)

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