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Handbook for clinical research = des...

Hammond, Flora.

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Handbook for clinical research = design, statistics, and implementation /

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Handbook for clinical research/ Flora Hammond, Jame F. Malec, Todd G. Nick, Ralph M. Buschbacher.
其他題名:	design, statistics, and implementation /
其他作者:	Hammond, Flora.
出版者:	[New York] :Demos Medical, : [2015],
面頁冊數:	1 online resource (348 p.)
內容註:	Handbook for clinical research: design, statistics, and implementation -- Contents -- Contributors -- Preface -- Share Handbook for Clinical Research: Design, Statistics, and Implementation --
內容註:	Part I: Design -- Chapter 1: Development and Testing of Treatments -- Chapter 2: Qualitative Research -- Chapter 3: Single-Case Experimental Designs -- Chapter 4: Studies of Associations -- Chapter 5: Observational Studies: Retrospective Versus Prospective -- Chapter 6: Historical Controls -- Chapter 7: Subject as Own Control -- Chapter 8: Longitudinal Cohort Versus Cross-Sectional Cohort Studies -- Chapter 9: Survey Research -- Chapter 10: Choice of Control Groups in Treatment Studies -- Chapter 11: Randomization -- Chapter 12: Special Issues in Randomized Controlled Trials -- Chapter 13: Secondary Data Analysis -- Chapter 14: Scoping Study -- Chapter 15: Systematic Reviews -- Chapter 16: Meta-Analysis -- Chapter 17: Recommendations for Reporting Research Studies -- Chapter 18: Developing and Evaluating Systematic Reviews and Practice Guidelines
內容註:	Part II: Statistics -- Chapter 19: Introduction -- Chapter 20: Types of Data -- Chapter 21: Descriptive Statistics -- Chapter 22: Data Distributions -- Chapter 23: Samples and Populations -- Chapter 24: Visual Display of Data -- Chapter 25: Data Cleaning -- Chapter 26: Missing Data and Imputation -- Chapter 27: Estimation -- Chapter 28: Hypothesis Testing -- Chapter 29: Sample Size and Power -- Chapter 30: Comparing Matched Samples With Continuous-Type Outcomes: Two Groups -- Chapter 31: Comparing Independent Samples With Continuous-Type Outcomes: Two Groups -- Chapter 32: Comparing Independent Samples for Continuous-Type Outcomes: Three Groups or More -- Chapter 33: Correlation -- Chapter 34: Simple Linear Regression -- Chapter 35: Multiple Linear Regression -- Chapter 36: Longitudinal and Clustered Data -- Chapter 37: Signifi cance Tests: Categorical Data -- Chapter 38: Measures of Effect Sizes for Categorical Outcomes -- Chapter 39: Logistic Regression -- Chapter 40: Kaplan-Meier Estimator --
內容註:	Chapter 41: Log-Rank Test -- Chapter 42: Proportional Hazards Model -- Chapter 43: Sources of Error: Selection Bias, Information Bias, and Confounding -- Chapter 44: Mediation Analyses -- Chapter 45: Epidemiology Study: Incidence and Prevalence -- Chapter 46: Validity and Performance of Screening: Sensitivity, Specificity, Positive Predictive Value, and Negative Predictive Value -- Chapter 47: Statistical Tools for Agreement and Reliability Studies -- Chapter 48: Classical Test Theory -- Chapter 49: Item Response Theory
內容註:	Part III: Implementation -- Chapter 50: Successful Grant Applications -- Chapter 51: Sources of Research Funding -- Chapter 52: Planning Grants -- Chapter 53: Developing the Idea With Stakeholder Input -- Chapter 54: Research Questions, Hypotheses, Aims, and Abstract -- Chapter 55: Reviewing the Literature -- Chapter 56: Background and Significance -- Chapter 57: Preliminary Studies and Experience -- Chapter 58: Methods and Design -- Chapter 59: Types of Measures -- Chapter 60: Letters of Support -- Chapter 61: Budget and Budget Justification -- Chapter 62: Preaward Management -- Chapter 63: Post-Award Management -- Chapter 64: Good Clinical Practices -- Chapter 65: Research Misconduct -- Chapter 66: Study Protocol -- Chapter 67: Manual of Procedures -- Chapter 68: Treatment Manuals -- Chapter 69: Participant Recruitment and Enrollment -- Chapter 70: Participant Retention --
內容註:	Chapter 71: Data Collection -- Chapter 72: Case Report Forms -- Chapter 73: Database Development -- Chapter 74: Data Dictionary -- Chapter 75: Data Management -- Chapter 76: Plan of Operation -- Chapter 77: Evaluation -- Chapter 78: Regulatory Binder and Essential Documents -- Chapter 79: Adverse Events -- Chapter 80: Protocol Deviations and Violations -- Chapter 81: Data and Safety Monitoring -- Chapter 82: Multicenter Trials -- Chapter 83: Site Monitoring and Oversight -- Index.
標題:	Biomedical Research. -
電子資源:	http://portal.igpublish.com/iglibrary/search/SPCB0001358.html
ISBN:	1936287544

Handbook for clinical research = design, statistics, and implementation /
Handbook for clinical researchdesign, statistics, and implementation /[electronic resource] :Flora Hammond, Jame F. Malec, Todd G. Nick, Ralph M. Buschbacher. - 1st ed. - [New York] :Demos Medical,[2015] - 1 online resource (348 p.)

Includes bibliographical references and index.

Handbook for clinical research: design, statistics, and implementation -- Contents -- Contributors -- Preface -- Share Handbook for Clinical Research: Design, Statistics, and Implementation --

ISBN: 1936287544

Source: 838067660001358Subjects--Topical Terms:

851895
Biomedical Research.

LC Class. No.: RC386.2 / .T57 2013

Dewey Class. No.: 616.805

Handbook for clinical research = design, statistics, and implementation /
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505 0 $a Handbook for clinical research: design, statistics, and implementation -- Contents -- Contributors -- Preface -- Share Handbook for Clinical Research: Design, Statistics, and Implementation --
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505 8 $a Part II: Statistics -- Chapter 19: Introduction -- Chapter 20: Types of Data -- Chapter 21: Descriptive Statistics -- Chapter 22: Data Distributions -- Chapter 23: Samples and Populations -- Chapter 24: Visual Display of Data -- Chapter 25: Data Cleaning -- Chapter 26: Missing Data and Imputation -- Chapter 27: Estimation -- Chapter 28: Hypothesis Testing -- Chapter 29: Sample Size and Power -- Chapter 30: Comparing Matched Samples With Continuous-Type Outcomes: Two Groups -- Chapter 31: Comparing Independent Samples With Continuous-Type Outcomes: Two Groups -- Chapter 32: Comparing Independent Samples for Continuous-Type Outcomes: Three Groups or More -- Chapter 33: Correlation -- Chapter 34: Simple Linear Regression -- Chapter 35: Multiple Linear Regression -- Chapter 36: Longitudinal and Clustered Data -- Chapter 37: Signifi cance Tests: Categorical Data -- Chapter 38: Measures of Effect Sizes for Categorical Outcomes -- Chapter 39: Logistic Regression -- Chapter 40: Kaplan-Meier Estimator --
505 8 $a Chapter 41: Log-Rank Test -- Chapter 42: Proportional Hazards Model -- Chapter 43: Sources of Error: Selection Bias, Information Bias, and Confounding -- Chapter 44: Mediation Analyses -- Chapter 45: Epidemiology Study: Incidence and Prevalence -- Chapter 46: Validity and Performance of Screening: Sensitivity, Specificity, Positive Predictive Value, and Negative Predictive Value -- Chapter 47: Statistical Tools for Agreement and Reliability Studies -- Chapter 48: Classical Test Theory -- Chapter 49: Item Response Theory
505 8 $a Part III: Implementation -- Chapter 50: Successful Grant Applications -- Chapter 51: Sources of Research Funding -- Chapter 52: Planning Grants -- Chapter 53: Developing the Idea With Stakeholder Input -- Chapter 54: Research Questions, Hypotheses, Aims, and Abstract -- Chapter 55: Reviewing the Literature -- Chapter 56: Background and Significance -- Chapter 57: Preliminary Studies and Experience -- Chapter 58: Methods and Design -- Chapter 59: Types of Measures -- Chapter 60: Letters of Support -- Chapter 61: Budget and Budget Justification -- Chapter 62: Preaward Management -- Chapter 63: Post-Award Management -- Chapter 64: Good Clinical Practices -- Chapter 65: Research Misconduct -- Chapter 66: Study Protocol -- Chapter 67: Manual of Procedures -- Chapter 68: Treatment Manuals -- Chapter 69: Participant Recruitment and Enrollment -- Chapter 70: Participant Retention --
505 8 $a Chapter 71: Data Collection -- Chapter 72: Case Report Forms -- Chapter 73: Database Development -- Chapter 74: Data Dictionary -- Chapter 75: Data Management -- Chapter 76: Plan of Operation -- Chapter 77: Evaluation -- Chapter 78: Regulatory Binder and Essential Documents -- Chapter 79: Adverse Events -- Chapter 80: Protocol Deviations and Violations -- Chapter 81: Data and Safety Monitoring -- Chapter 82: Multicenter Trials -- Chapter 83: Site Monitoring and Oversight -- Index.
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650 2 2 $a Epidemiologic Research Design. $3 3240985
650 2 2 $a Statistics as Topic. $3 2017472
700 1 $a Hammond, Flora. $3 3240981
700 1 $a Malec, Jame F., $e author $3 3240982
700 1 $a Nick, Todd G., $e author $3 3240983
700 1 $a Buschbacher, Ralph M., $e author $3 3240984
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