跳至主要内容
临床试验/NCT04854629
NCT04854629已完成不适用

Effects of the "Spinomed Active" Orthosis on Chronic Back Pain in Women With Osteoporotic Vertebral Bone Fracture and Hyperkyphosis.

University of Erlangen-Nürnberg Medical School1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2021年4月7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
80
试验地点
1
主要终点
Back pain

研究概览

简要总结

Osteoporotic vertebral fractures often lead to postural changes, chronic spinal pain conditions and limited functionality. Orthoses that straighten the spine have been shown in studies to have a positive effect on pain, posture and the functional state of patients with a fresh vertebral fracture.

The planned study investigates the effect of the orthosis "Spinomed active" in patients aged ≥ 65 years with at least one non-acute osteoporotic vertebral fracture (at least 3 months ago) and chronic back pain.

研究设计

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

盲法说明

Outcomes assessor were unaware of participant status (i.e. spinomed active or control) and were not allowed to ask correspondingly

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Living independently in the community
  • •≥ 1 low-traumatic vertebral fracture ≥ 3 months ago
  • •Chronic back pain according to the national guideline for low back pain
  • •Mean back pain intensity NPS ≥ 1 (1-10 scale)
  • •Hyperkyphosis, kyphosis angle according to Debrunner >40°
  • •Intact skin or adequate wound coverage in the area of the contact surface of the orthosis

排除标准

  • •Secondary osteoporosis (as determined by study physician)
  • •Expected change in overall pain therapy during the study period
  • •Structurally fixed kyphosis, lack of extension ability of the thoracic spine
  • •Kyphoplasty, vertebroplasty
  • •Use of back orthoses during the last 6 months
  • •Depression
  • •Dementia, cognitive impairment (Mini Mental Test < 25)
  • •Fresh neurological deficits; incontinence > grade 1
  • •Body dimensions that do not allow for adjustment of the back orthosis
  • •Absence during baseline and follow-up assessments

研究组 & 干预措施

Spinomed active orthosis

Experimental

Wearing the orthosis for 16 weeks

干预措施: Spinomed active (Other)

Control group

No Intervention

No intervention: non spinomed active control

结局指标

主要结局

Back pain

时间窗: At baseline and after 16 weeks (i.e. over 16 weeks)

Change in back pain (mean intensity over 4 weeks on the "numeric pain scale (NPS) "0-10").

次要结局

  • Kyphosis angle(At baseline and after 16 weeks (i.e. over 16 weeks))
  • Trunk strength/performance(At baseline and after 16 weeks (i.e. over 16 weeks))
  • Functional capacity(At baseline and after 16 weeks (i.e. over 16 weeks))
  • Everyday life skills(At baseline and after 16 weeks (i.e. over 16 weeks))
  • Pulmonary function(At baseline and after 16 weeks (i.e. over 16 weeks))
  • Balance capacity(At baseline and after 16 weeks (i.e. over 16 weeks))

研究者

发起方
University of Erlangen-Nürnberg Medical School
申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验