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临床试验/NCT07701356
NCT07701356已完成不适用

Effects of Joint Mobilization on Hand Function in Patients With Stiff Hand: A Randomized Controlled Trial

Pamukkale University1 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2025年1月24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
入组人数
34
试验地点
1
主要终点
Range of Motion

研究概览

简要总结

Although various treatment modalities have been investigated for the management of stiff hand, no previous study has examined the combined use of exercise and joint mobilization. Therefore, the present study was designed to investigate the effects of peripheral joint mobilization, applied in addition to conventional exercise, on functional outcomes in patients with stiff hand.

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
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Hand or forearm injury managed conservatively or surgically
  • Stiff hand criteria confirmed by Modified Weeks Test (0-20° difference between pre- and post-conditioning passive ROM)
  • No communication impairment
  • No prior neurological, orthopedic, or rheumatological condition or surgery in the affected extremity

排除标准

  • Circulatory disorder or Complex Regional Pain Syndrome
  • Dupuytren's disease
  • Acute inflammation in any finger within the last week
  • Fracture due to non-traumatic causes
  • Significant edema

研究组 & 干预措施

Joint mobilization with conventional physiotherapy

Experimental

干预措施: Joint Mobilization with Conventional Physiotherapy (Other)

Conventional Physiotherapy Only

Active Comparator

干预措施: Conventional Physiotherapy Only (Other)

结局指标

主要结局

Range of Motion

时间窗: Assessments were performed at baseline, at the end of treatment (4 weeks), and at the 8-week follow-up.

Total Active Motion (TAM) assessed by metal finger goniometer.

Grip Strength

时间窗: Assessments were performed at baseline, at the end of treatment (4 weeks), and at the 8-week follow-up.

Grip Strength was assessed by Jamar dynamometer (gross grip, pinch, pulp, lateral, tripod)

次要结局

  • Michigan Hand Outcomes Questionnaire(Assessments were performed at baseline, at the end of treatment (4 weeks), and at the 8-week follow-up.)

研究者

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

UMUT ERASLAN

Assistant Professor

Pamukkale University

研究点 (1)

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