RATER RESOURCE ALLOCATION SYSTEMS AND METHODS
    1.
    发明申请
    RATER RESOURCE ALLOCATION SYSTEMS AND METHODS 审中-公开
    RATER资源分配系统和方法

    公开(公告)号:US20090198504A1

    公开(公告)日:2009-08-06

    申请号:US12025871

    申请日:2008-02-05

    IPC分类号: G06Q10/00

    摘要: Methods of allocating raters to assessment visits of studies, and tangible computer readable media including software that is adapted to control a computer to implement methods of allocating raters to assessment visits of studies, are provided. Raters are allocated by retrieving blinding information that includes at least one blinding criterion for a visit of a study, retrieving rater information for at least one rater associated with the study, comparing the retrieved rater information and the retrieved blinding information to identify one or more raters meeting the at least one blinding criterion and enabling selection of the identified one or more raters for allocation to the visit of the study. A rater may then be allocated to the visit by receiving a selection for at least one of the identified raters and allocating the at least one rater to the visit responsive to the received selection.

    摘要翻译: 提供了将评估者分配给研究评估访问的方法,以及包括软件的有形计算机可读介质,该软件适用于控制计算机实施将评估者分配给研究评估访问的方法。 评估者通过检索包含研究访问的至少一个盲目标准的盲目信息来分配,检索与研究相关联的至少一个评分者的评估者信息,比较检索到的评分信息和检索到的盲法信息以识别一个或多个评估者 满足至少一个致盲标准,并且能够选择所识别的一个或多个评估者用于分析研究的访问。 然后可以通过接收对所识别的评估者中的至少一个的选择并将响应于所接收的选择的至少一个评估者分配给访问来将评分者分配给访问。

    RATER RESOURCE ALLOCATION SYSTEMS AND METHODS
    4.
    发明申请
    RATER RESOURCE ALLOCATION SYSTEMS AND METHODS 审中-公开
    RATER资源分配系统和方法

    公开(公告)号:US20120084093A1

    公开(公告)日:2012-04-05

    申请号:US13222166

    申请日:2011-08-31

    IPC分类号: G06Q50/22

    摘要: Methods of allocating raters to assessment visits of studies, and tangible computer readable media including software that is adapted to control a computer to implement methods of allocating raters to assessment visits of studies, are provided. Raters are allocated by retrieving blinding information that includes at least one blinding criterion for a visit of a study, retrieving rater information for at least one rater associated with the study, comparing the retrieved rater information and the retrieved blinding information to identify one or more raters meeting the at least one blinding criterion and enabling selection of the identified one or more raters for allocation to the visit of the study. A rater may then be allocated to the visit by receiving a selection for at least one of the identified raters and allocating the at least one rater to the visit responsive to the received selection.

    摘要翻译: 提供了将评估者分配给研究评估访问的方法,以及包括软件的有形计算机可读介质,该软件适用于控制计算机实施将评估者分配给研究评估访问的方法。 评估者通过检索包含研究访问的至少一个盲目标准的盲目信息来分配,检索与研究相关联的至少一个评分者的评估者信息,比较检索到的评分信息和检索到的盲法信息以识别一个或多个评估者 满足至少一个致盲标准,并且能够选择所识别的一个或多个评估者用于分析研究的访问。 然后可以通过接收对所识别的评估者中的至少一个的选择并将响应于所接收的选择的至少一个评估者分配给访问来将评分者分配给访问。

    SYSTEM AND METHOD FOR FACILITATING CANDIDATE AND SUBJECT PARTICIPATION IN CLINICAL TRIAL STUDIES
    5.
    发明申请
    SYSTEM AND METHOD FOR FACILITATING CANDIDATE AND SUBJECT PARTICIPATION IN CLINICAL TRIAL STUDIES 审中-公开
    在临床试验研究中促进候选人和参与参与的系统和方法

    公开(公告)号:US20120084100A1

    公开(公告)日:2012-04-05

    申请号:US13312040

    申请日:2011-12-06

    IPC分类号: G06Q50/22 G06Q50/24

    摘要: The present invention discloses systems and methods for facilitating candidate and subject participation in clinical trial studies. Medical professionals participating in the study at satellite sites assist in recruitment of their pre-existing patients as subjects in the study. Clinical trial data collected from the subjects is communicated over a computer network from the satellite sites to core sites. Study coordination is performed at the core sites. The collected clinical trial data is analyzed in accordance with the study at an interested party site.

    摘要翻译: 本发明公开了用于促进候选人和受试者参与临床试验研究的系统和方法。 在卫星地点参与研究的医疗专业人员可以协助招募其先前存在的患者作为研究对象。 从受试者收集的临床试验数据通过计算机网络从卫星站点传送到核心站点。 在核心地点进行学习协调。 收集的临床试验数据根据感兴趣的场所的研究进行分析。

    SYSTEM AND METHOD FOR FACILITATING CENTRALIZED CANDIDATE SELECTION AND MONITORING SUBJECT PARTICIPATION IN CLINICAL TRIAL STUDIES
    6.
    发明申请
    SYSTEM AND METHOD FOR FACILITATING CENTRALIZED CANDIDATE SELECTION AND MONITORING SUBJECT PARTICIPATION IN CLINICAL TRIAL STUDIES 审中-公开
    促进中心候选人选择和监测临床试验研究中的主体参与的系统和方法

    公开(公告)号:US20110077962A1

    公开(公告)日:2011-03-31

    申请号:US12963765

    申请日:2010-12-09

    IPC分类号: G06Q50/00 G06Q10/00

    摘要: A system and method of facilitating centralized and standardized remote ratings of subjects in clinical trial studies includes providing training to raters located at one or more central rating sites such that the raters are trained to apply substantially similar criteria in determining whether a candidate is a qualified subject for the clinical trial and/or in the actual assessment, or information collection, phase of the clinical trail. By having centralized, consistently trained raters that are independent of clinical trial investigators, inter-rater reliability is enhanced and potential bias is reduced, thus increasing the effectiveness of the clinical trial results by providing more qualified subjects and more accurate results.

    摘要翻译: 在临床试验研究中促进受试者的集中和标准化远程评级的系统和方法包括向位于一个或多个中心评价点的评估者提供培训,使得评估者被训练以在确定候选人是否合格的受试者时应用基本相似的标准 用于临床试验和/或实际评估,或信息收集阶段的临床踪迹。 通过拥有独立于临床试验研究者的集中,一致训练的评估者,提高了评估者的可靠性,减少潜在的偏差,从而通过提供更多的合格科目和更准确的结果来提高临床试验结果的有效性。

    SYSTEM AND METHOD FOR FACILITATING CANDIDATE AND SUBJECT PARTICIPATION IN CLINICAL TRIAL STUDIES
    7.
    发明申请
    SYSTEM AND METHOD FOR FACILITATING CANDIDATE AND SUBJECT PARTICIPATION IN CLINICAL TRIAL STUDIES 审中-公开
    在临床试验研究中促进候选人和参与参与的系统和方法

    公开(公告)号:US20100250288A1

    公开(公告)日:2010-09-30

    申请号:US12815966

    申请日:2010-06-15

    IPC分类号: G06Q50/00 G06F17/30

    摘要: The present invention discloses systems and methods for facilitating candidate and subject participation in clinical trial studies. Medical professionals participating in the study at satellite sites assist in recruitment of their pre-existing patients as subjects in the study. Clinical trial data collected from the subjects is communicated over a computer network from the satellite sites to core sites. Study coordination is performed at the core sites. The collected clinical trial data is analyzed in accordance with the study at an interested party site.

    摘要翻译: 本发明公开了用于促进候选人和受试者参与临床试验研究的系统和方法。 在卫星地点参与研究的医疗专业人员可以协助招募其先前存在的患者作为研究对象。 从受试者收集的临床试验数据通过计算机网络从卫星站点传送到核心站点。 在核心地点进行学习协调。 收集的临床试验数据根据感兴趣的场所的研究进行分析。

    SYSTEM AND METHOD FOR FACILITATING CENTRALIZED CANDIDATE SELECTION AND MONITORING SUBJECT PARTICIPATION IN CLINICAL TRIAL STUDIES
    8.
    发明申请
    SYSTEM AND METHOD FOR FACILITATING CENTRALIZED CANDIDATE SELECTION AND MONITORING SUBJECT PARTICIPATION IN CLINICAL TRIAL STUDIES 审中-公开
    促进中心候选人选择和监测临床试验研究中的主体参与的系统和方法

    公开(公告)号:US20100100397A1

    公开(公告)日:2010-04-22

    申请号:US12643594

    申请日:2009-12-21

    IPC分类号: G06Q50/00

    摘要: A system and method of facilitating centralized and standardized remote ratings of subjects in clinical trial studies includes providing training to raters located at one or more central rating sites such that the raters are trained to apply substantially similar criteria in determining whether a candidate is a qualified subject for the clinical trial and/or in the actual assessment, or information collection, phase of the clinical trail. By having centralized, consistently trained raters that are independent of clinical trial investigators, inter-rater reliability is enhanced and potential bias is reduced, thus increasing the effectiveness of the clinical trial results by providing more qualified subjects and more accurate results.

    摘要翻译: 在临床试验研究中促进受试者的集中和标准化远程评级的系统和方法包括向位于一个或多个中心评价点的评估者提供培训,使得评估者被训练以在确定候选人是否合格的受试者时应用基本相似的标准 用于临床试验和/或实际评估,或信息收集阶段的临床踪迹。 通过拥有独立于临床试验研究者的集中,一致训练的评估者,提高了评估者的可靠性,减少潜在的偏差,从而通过提供更多的合格科目和更准确的结果来提高临床试验结果的有效性。

    System and method for facilitating candidate and subject participation in clinical trial studies
    9.
    发明申请
    System and method for facilitating candidate and subject participation in clinical trial studies 审中-公开
    促进候选人和受试者参与临床试验研究的系统和方法

    公开(公告)号:US20090150187A1

    公开(公告)日:2009-06-11

    申请号:US12288634

    申请日:2008-10-21

    摘要: The present invention discloses systems and methods for facilitating candidate and subject participation in clinical trial studies. Medical professionals participating in the study at satellite sites assist in recruitment of their pre-existing patients as subjects in the study. Clinical trial data collected from the subjects is communicated over a computer network from the satellite sites to core sites. Study coordination is performed at the core sites. The collected clinical trial data is analyzed in accordance with the study at an interested party site.

    摘要翻译: 本发明公开了用于促进候选人和受试者参与临床试验研究的系统和方法。 在卫星地点参与研究的医疗专业人员可以协助招募其先前存在的患者作为研究对象。 从受试者收集的临床试验数据通过计算机网络从卫星站点传送到核心站点。 在核心地点进行学习协调。 收集的临床试验数据根据感兴趣的场所的研究进行分析。

    SYSTEM AND METHOD FOR FACILITATING CENTRALIZED CANDIDATE SELECTION AND MONITORING SUBJECT PARTICIPATION IN CLINICAL TRIAL STUDIES
    10.
    发明申请
    SYSTEM AND METHOD FOR FACILITATING CENTRALIZED CANDIDATE SELECTION AND MONITORING SUBJECT PARTICIPATION IN CLINICAL TRIAL STUDIES 审中-公开
    促进中心候选人选择和监测临床试验研究中的主体参与的系统和方法

    公开(公告)号:US20090132288A1

    公开(公告)日:2009-05-21

    申请号:US12349730

    申请日:2009-01-07

    IPC分类号: G06Q50/00

    摘要: A system and method of facilitating centralized and standardized remote ratings of subjects in clinical trial studies includes providing training to raters located at one or more central rating sites such that the raters are trained to apply substantially similar criteria in determining whether a candidate is a qualified subject for the clinical trial and/or in the actual assessment, or information collection, phase of the clinical trail. By having centralized, consistently trained raters that are independent of clinical trial investigators, inter-rater reliability is enhanced and potential bias is reduced, thus increasing the effectiveness of the clinical trial results by providing more qualified subjects and more accurate results.

    摘要翻译: 在临床试验研究中促进受试者的集中和标准化远程评级的系统和方法包括向位于一个或多个中心评价点的评估者提供培训,使得评估者被训练以在确定候选人是否合格的受试者时应用基本相似的标准 用于临床试验和/或实际评估,或信息收集阶段的临床踪迹。 通过拥有独立于临床试验研究者的集中,一致训练的评估者,提高了评估者的可靠性,减少潜在的偏差,从而通过提供更多的合格科目和更准确的结果来提高临床试验结果的有效性。