The Role of Patient Expectations in Traumatic Orthopedic Outcomes-TEFTOM EURASIA
The Role of Patient Expectations in Traumatic Orthopedic Outcomes TEFTOM: The Trauma Expectation Factor - Trauma Outcomes Measure TEFTOM EURASIA
Design:
Prediction trial, up to 10 sites in Asia and Europe
Goal:
To better understand the "success" or "failure" after orthopedic trauma surgery by developing a model that can be applied clinically as a user-friendly "baseline" questionnaire - capable of predicting "success" or "failure" based on a patient's pre-surgical expectations of their final outcome and to validate a novel outcomes measure (TOM).
Primary aim:
To assess the psychometric properties of predictive validity, internal consistency and reproducibility of the trauma expectation factor (TEF) in the Eurasian population.
Secondary aim:
To assess the psychometric properties of criterion validity, internal consistency,reproducibility, and sensitivity to change of the TOM in the Eurasian population.
Key questions related to patient and surgeon expectations:
- How different, or similar, are patient and surgeon expectations?
- Do expectations change over time?
- Do patient expectations predict outcomes in validated measures use today?
研究概览
研究类型
注册 (实际的)
联系人和位置
学习地点
-
-
-
Hong Kong、中国
- Queen Mary Hospital
-
Shanghai、中国、200233
- Shanghai Sixth People's Hospital
-
-
-
-
-
Bangalore、印度、560025
- HOSMAT Hospital
-
-
-
-
-
Köln、德国、50931
- Universitätsklinikum Köln
-
-
-
-
-
Luzern、瑞士、6000
- Kantonsspital Luzern
-
Zürich、瑞士、8063
- Stadtspital Triemli
-
-
-
-
-
Girona、西班牙、17007
- Hospital Universitari de Girona Doctor Josep Trueta
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
描述
Inclusion Criteria:
- Isolated ankle or distal tibia fracture
Scheduled for and undergoing one of the following surgeries for their fracture:
- Open fracture and internal fixation (ORIF)
- external fixation (EF)
- EF followed by ORIF
- 18 years of age or older
- Understand and read country national language at elementary level
- Able to understand the purpose of the clinical trial,
- Able and willing to conduct all follow-up visits
- Signed informed consent
Exclusion Criteria:
- Subject has previously undergone internal fixation surgery for this ankle/distal tibia fracture.
- Subject has disease entity, or condition that precludes likelihood of bony union (e.g., metastatic cancer, metabolic bone disease).
- Subject has severe dementia or other severe mental health problem that may preclude him/her from completing study questionnaires.
- Subject is participating in other competing clinical research that may interfere with participation in this research.
- Subject is unlikely to attend study related follow-up visits.
- Subject has poly-trauma (more than one organ system compromised)
- Subject has additional fracture(s) other than ankle fracture
- Subject is a prisoner
- Fracture occurred more than 28 days before surgery
学习计划
研究是如何设计的?
设计细节
队列和干预
团体/队列 |
---|
TEFTOM
Patient outcome measure
|
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
---|---|
Teftom Questionnaire
大体时间:one year
|
one year
|
合作者和调查者
调查人员
- 首席研究员:Reto Babst, MD、Luzerner Kantonsspital
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.