SCOPE and Special Olympics (SCOPE/SO)
2017年10月11日 更新者:Texas Woman's University
The purpose of this study is to examine if Special Olympic athletes's life participation improves through involvement with Special Olympics.
This project will be undertaken in coordination with Special Olympics entities from Texas and around the nation to determine how involvement in Special Olympics improves the strengths and limitations of their athletes.
The Short Child Occupational Profile (SCOPE) will be used to gather this information from the parents and coaches.
The SCOPE measures the impact that personal and environmental factors have on a child or youth's occupational participation.
研究概览
详细说明
The research team members will not have contact with the Special Olympic athletes.
Parents and coaches will be the only individuals who have contact with the athletes.
Participants will be assured that their participation is completely voluntary.
If they agree to participate in the research an informed assest form will be explained by a parent, guardian, or coach and they will be asked to sign it.
Parents will be asked to sign a consent form for their child's participation in the study.
Coaches will administer the SCOPE as a pre/post-test outcome measure.
Parents will submit the Parent form of the SCOPE and the coaches will submit the SCOPE Clinical Data Summary Form.
All data will be de-identified and sent in form the coaches.
The TWU special olympics research team will compile de-identified data from a pre-test and post-test utilizing the SCOPE.
A codebook that links the ID number with the participants will be kept by the coaches.
The research team may be able to trace assented data collected through the TWU data collection protocol back to the coaches.
Participating athletes will not be contacted by the PI and no contact information will be collected.
In the case of an unexpected or adverse event, or if the participants request to be contacted, attempts may be made to find the subjects contact information through the coaches.
De-identified data collected by the TWU Special Olympic research team or other Key Research personnel will be stored on a password protected computer or in a locked file cabinet in a locked office in the department of occupational therapy at Texas Woman's University in Houston.
The raw data collected will not be made available to anyone other than the PI and immediate study research personnel.
Data is entered into the database using the ID number, and the computer database is password protected.
The raw data is not going to be shared.
The data will be kept in a locked file cabinet within the research office of the databases destroyed 4 years after the end of the study.
The results of the analysis, which may include information from the data, will be kept on a password secure computer indefinitely.
The data collected from pre-tests and post-tests will then be compiled and analyzed.
研究类型
观察性的
注册 (实际的)
1
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
-
-
Texas
-
Houston、Texas、美国
- Texas Woman's University
-
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参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
7年 及以上 (孩子、成人、年长者)
接受健康志愿者
不
有资格学习的性别
全部
取样方法
非概率样本
研究人群
Participating athletes will be recruited through the coaches.
Participants recruited under the TWU collection protocol will be informed that they are being asked to be a subject in a research study to determine if there is a change in levels of participation in other areas of life for athletes involved in special olympics.
描述
Inclusion Criteria:
- new members (within 2 years),
- English-speaking,
- U.S. citizens, and
- must be 7 years or older at the time of assess.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
队列和干预
团体/队列 |
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Special Olympic athletes
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
---|---|---|
Short Child Occupational Profile
大体时间:up to 3 years-estimated
|
To determine if there is a change in levels of participation in other areas of life for athletes involved in Special Olympics
|
up to 3 years-estimated
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员:Patricia Bowyer, EdD, OTR, BCN, FAOTA、Texas Woman's University
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2010年5月1日
初级完成 (实际的)
2013年6月1日
研究完成 (实际的)
2016年11月1日
研究注册日期
首次提交
2013年7月5日
首先提交符合 QC 标准的
2013年7月10日
首次发布 (估计)
2013年7月11日
研究记录更新
最后更新发布 (实际的)
2017年10月13日
上次提交的符合 QC 标准的更新
2017年10月11日
最后验证
2013年7月1日
更多信息
与本研究相关的术语
其他研究编号
- 15528
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.