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临床试验/NCT00462683
NCT00462683已完成不适用

Bone Loss, Fractures, and Management of Bone Health in People With Stroke in Managed Rehabilitation Settings

Northwestern University2 个研究点 分布在 1 个国家目标入组 87 人开始时间: 2007年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
87
试验地点
2

研究概览

简要总结

The purpose of the study is to evaluate the state of bone health of brain injury patients being seen within a rehabilitation setting. Osteopenia is a condition of bone in which decreased calcification, decreased density, or reduced mass occurs. Osteoporosis is a disease in which the bones become extremely porous, are subject to fracture, and heal slowly. More specifically, the prevalence of osteopenia and osteoporosis at specific anatomic locations (e.g., forearms, hips, spine) will be determined as will specific interventions (e.g., use of vitamins, nutritional supplements, specific prescription medications) that people with brain injury may be applying, or have applied, to manage their bone health. An attempt will also be made to evaluate severity of brain injury, based on loss of muscle strength/function, and to compare this data with bone-focused information such as bone mineral density (BMD), falls, and history.

详细描述

Primary Outcomes: As this study has no control or comparator group, the goal will be to provide descriptive data regarding the prevalence of osteopenia and osteoporosis at each of the anatomic sites evaluated by DEXA in this specialized population (BMD outcome measures). Additionally, the use of bone-specific interventions (vitamins, nutritional supplements, medications), previous diagnostic testing (DEXA) and history of falls and fractures will be assessed to determine the extent to which bone health has been considered and evaluated in this population of individuals at increased risk of fracture.

Secondary Outcomes: Functional status measures will also be obtained to enable correlation with bone data.

This study involves a cross-sectional, descriptive evaluation of a cohort of 225 patients with brain injury who are being managed at the out-patient clinics by physicians from RIC. The goal of the study is to provide representative data of both the general bone health of this population of patients (degree, extent and localization of bone loss) as well as interventions that may have been implemented to manage their bone health (vitamins, nutritional supplements, prescription medications). After obtaining informed consent, those patients who wish to be involved will be asked to complete a medical history questionnaire that focuses on bone health and will then undergo measurement of bone density by DEXA (dual energy X-ray absorptiometry). At the time of the DEXA examination, muscle strength will be evaluated by a trained research coordinator. A dietary history and a blood sample will also be obtained, the latter for storage in order to later measure vitamin D levels and/or other bone markers. All subjects will then be given the opportunity to continue in the longitudinal arm of the study (second phase). Those who do will sign the informed consent and will then be re-evaluated at yearly intervals with the same set of data being obtained.

Descriptive Data to be Obtained:

  1. Demographics: date of birth, sex, race, ethnicity
  2. Detailed and complete medical history, with particular focus on:

研究设计

研究类型
Observational
时间视角
Prospective

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

  • History of brain injury at some defined time in the past (include stroke, traumatic brain injury, anoxia)
  • Age 16 years and older (no upper age limit)
  • Male and females
  • Able to undergo a DEXA examination (able to lie on the DEXA table for 20-30 minutes)
  • Able to provide answers to the questionnaires regarding medical and dietary history and demographics
  • Able to provide informed consent

排除标准

  • History of spinal cord injury
  • History of traumatic brain damage
  • Inability to lie down appropriately to obtain DEXA measurements
  • Inability to communicate
  • Anything condition that in the judgment of the physician would prevent the person from participating

研究者

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

Thomas J. Schnitzer

professor

Northwestern University

研究点 (2)

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