Single case experimental designs : strategies for studying behavior for change /

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Bibliographic Details
Author / Creator:Barlow, David H.
Edition:3rd ed.
Imprint:Boston : Pearson/Allyn and Bacon, c2009.
Description:xvi, 393 p. : ill. ; 23 cm.
Language:English
Subject:
Format: Print Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/7182666
Hidden Bibliographic Details
Other authors / contributors:Nock, Matthew.
Hersen, Michel.
ISBN:9780205474554
0205474551
Notes:Includes bibliographical references (p. 347-373) and indexes.
Table of Contents:
  • Preface
  • Epigram
  • Chapter 1. The Single Case in Basic and Applied Research: An Historical Perspective
  • 1.1. Introduction
  • 1.2. Beginnings in Experimental Physiology and Psychology
  • 1.3. Origins of the Group Comparison Approach
  • The influence of inferential statistics
  • 1.4. Development of Applied Research: The Case Study Method
  • Early reports of percentage of success in treated groups
  • The development of the group comparison approach in applied research
  • 1.5. Limitations of Early Group Comparison Approaches
  • Ethical objections and practical problems
  • Averaging of results
  • Generality of findings
  • Intersubject variability
  • 1.6. Early Alternative Approaches to Applied Research
  • Naturalistic studies
  • Process research
  • 1.7. The Scientist-Practitioner Split
  • 1.8. A Return to the Individual
  • The role of the case study
  • The representative case
  • Shapiro's methodology in the clinic
  • Quasi-experimental designs
  • Chassan and intensive designs
  • 1.9. The Experimental Analysis of Behavior
  • Chapter 2. General Issues in a Single-Case Approach
  • 2.1. Introduction
  • 2.2. Variability
  • Variability in basic research
  • Variability in applied research
  • Clinical vs. statistical significance
  • Highlighting variability in the individual
  • Repeated measures
  • Rapidly changing designs
  • 2.3. Experimental Analysis of Sources of Variability Through Improvised Designs
  • Subject fails to improve
  • Subject improves "spontaneously"
  • Subject displays cyclical variability
  • Searching for "hidden" sources of variability
  • 2.4. Behavior Trends and Intrasubject Averaging
  • 2.5. Relation of Variability to Generality of Findings
  • 2.6. Generality of Findings
  • Types of generality
  • Problems in generalizing from a single-case
  • 2.7. Some Limitations of Group Designs in Establishing Generality of Findings
  • Random sampling and inference in applied research
  • Problems in generalizing from the group to the individual
  • Improving generality of findings to the individual through homogeneous groups: logical generalization
  • 2.8. Homogeneous Groups Versus Replication of a Single-Case Experiment
  • Direct replication and treatment/no-treatment control group design
  • Systematic and clinical replication and factorial designs
  • 2.9. Blurring the Distinction Between Design Options
  • Chapter 3. General Procedures in Single-Case Research
  • 3.1. Introduction
  • 3.2. Repeated Measurement
  • Practical implications and limitations
  • 3.3. Choosing a Baseline
  • Baseline stability
  • Examples of baselines
  • 3.4. Changing One Variable at a Time
  • Correct and incorrect applications
  • Exceptions to the rule
  • Issues in drug evaluation
  • 3.5. Reversal and Withdrawal
  • The reversal design
  • Reversal and withdrawal designs compared
  • Withdrawal of treatment
  • Limitations and problems
  • 3.6. Length of Phases
  • Individual and relative length
  • Carryover effects
  • Cyclic variation
  • 3.7. Evaluation of Irreversible Procedures
  • Exceptions
  • 3.8. Assessing Response Maintenance
  • Chapter 4. Behavior Assessment
  • 4.1. Selection of Behavior to Assess
  • Social significance
  • Clinical significance
  • Organizational significance
  • Personal significance
  • 4.2. Measurement of Behavior
  • Primary measures: behavioral dimensionals of proximal, directly observed behavior
  • Temporality dimensions
  • Repeatability dimensions
  • Products of behavior
  • Behavior rating scales
  • Self-reports
  • Physiological measures
  • 4.3. Settings for Assessment
  • Contrived versus naturalistic settings and observations
  • A continuum of contrivance
  • Defining the behaviors to be observed
  • Selecting observers
  • Technically enhanced observation
  • Training observers
  • Reliability and validity
  • 4.4. The Assessment of Function
  • 4.5. Summary and Conclusions
  • Chapter 5. Basic A-B-A Withdrawal Designs
  • 5.1. Introduction
  • Limitations of the case study approach
  • 5.2. A-B Design
  • A-B with follow-up
  • A-B with multiple target measures and follow-up
  • A-B with follow-up and booster treatment
  • 5.3. A-B-A Design
  • A-B-A from the adult literature
  • A-B-A from child literature
  • 5.4. A-B-A-B Design
  • A-B-A-B from child literature
  • A-B-A-B when phase change is not under complete experimental control
  • A-B-A-B with unexpected improvement in baseline
  • A-B-A-B with monitoring of concurrent behaviors
  • A-B-A-B with no feedback to experimenter
  • 5.5. B-A-B Design
  • B-A-B with group data
  • B-A-B from rogerian framework
  • 5.6. A-B-C-B Design
  • A-B-C-B from the child literature
  • A-B-C-B in a group application and follow-up
  • Chapter 6. Extensions of the A-B-A Design, Uses in Drug Evaluation and Interaction Design Strategies
  • 6.1. Extensions and Variations of the A-B-A Withdrawal Design
  • 6.2. A-B-A-B-A-B Design
  • 6.3. Comparing Separate Treatment Variables/Components
  • A-B-A-C-A-C'-A design
  • 6.4. Parametric Variations of the Same Treatment Variable/Component
  • A-B-A-B-B[subscript 1]-B[subscript 2]-B[subscript 3]-B[subscript N] design
  • A-B- B[subscript 1]-B[subscript 2]-A-B[subscript 1] design
  • 6.5. Drug Evaluations
  • Issues specific to drug evaluations
  • Design options
  • 6.6. Strategies for Studying Interaction Effects
  • 6.7. Changing Criterion Designs
  • Chapter 7. Multiple Baseline Designs
  • 7.1. Introduction
  • 7.2. Multiple Baseline Designs
  • Types of multiple baseline designs
  • Multiple baseline design across behaviors
  • Multiple baseline design across subjects
  • Multiple baseline across settings
  • 7.3. Variations of Multiple Baseline Designs
  • Nonconcurrent multiple baseline design
  • Multiple-probe technique
  • 7.4. Issues in Drug Evaluations
  • Chapter 8. Alternating Treatments Design
  • 8.1. Introduction
  • History and terminology
  • 8.2. Procedural Considerations
  • Multiple-treatment interference
  • Counterbalancing relevant experimental factors
  • Number and sequencing of alternations
  • 8.3. Examples of Alternating Treatments Designs
  • Comparing treatment and no treatment conditions
  • Comparing multiple treatments
  • 8.4. Advantages of the Alternating Treatments Design
  • 8.5. Visual Analysis of the Alternating Treatments Designs
  • 8.6. Simultaneous Treatment Design
  • Chapter 9. Statistical Analyses for Single-Case Experimental Designs
  • 9.1. Introduction and Overview
  • 9.2. Single-Subject Experiments and Time-Series Data
  • The nature of time-series data
  • Mathematical and graphical description of a time series
  • The problem of autocorrelation
  • Autocorrelation and human behavior
  • General comments
  • 9.3. Specific Statistical Tests
  • Conventional t and F tests
  • Randomization tests
  • Interrupted time-series analysis (ITSA)
  • Autoregressive Integrated Moving Average (ARIMA) Models
  • Model building process
  • Intervention (impact) analysis
  • ITSA modeling strategies
  • Box-Jenkins-Tiao strategy (Box & Tiao, 1965)
  • Full series modeling strategy
  • Interrupted time-series experiment (ITSE)
  • Example
  • Intervention analysis
  • Other statistical tests
  • Revusky's R[subscript n] (test of ranks)
  • Split-middle technique
  • Double bootstrap method
  • Evaluation of statistical tests: which test to choose?
  • 9.4. Summary and Conclusion
  • Chapter 10. Beyond the Individual: Direct, Systematic, and Clinical Replication Procedures
  • 10.1. Introduction
  • 10.2. Direct Replication
  • Definition of direct replication
  • Example 1. two successful replications
  • Example 2. four successful replications with design alterations during replications
  • Example 3. mixed results in a multiple baseline design
  • Example 4. simultaneous replication in a group
  • Guidelines for direct replication
  • 10.3. Systematic Replication
  • Definition of systematic replication
  • Example: differential attention in children
  • Comment on replication
  • Guidelines for systematic replication
  • 10.4. Clinical Replication
  • Definition of clinical replication
  • Example: clinical replication with autistic children
  • 10.5. Benchmarking
  • 10.6. Practice Research Networks
  • 10.7. Advantages of Replication of Single-Case Experiments
  • Hiawatha Designs an Experiment
  • References
  • Subject Index
  • Name Index