The FIDL is a 21-item self-report questionnaire measuring cognitive and behavioral flexibility across five dimensions in daily life contexts, validated in adults aged 19-78 years with 10-15 minute administration time.
The scale demonstrates good psychometric properties (total α = .85) and unique sensitivity to lifespan changes, showing U-shaped relationships with age for total score and several subscales, with peak flexibility in middle adulthood.
Unlike laboratory-based measures, the FIDL provides ecologically valid assessment of real-world flexibility suitable for transdiagnostic clinical applications across neurodevelopmental, neurodegenerative, acquired brain injury, and psychiatric populations.
Introduction
The Flexibility in Daily Life scale (FIDL) is a 21-item self-report questionnaire designed to capture natural expressions of cognitive and behavioral flexibility in daily life. Developed by Horne, Chen, and Irish (2024), this scale measures the capacity to switch between task sets or adopt alternative viewpoints and to flexibly engage in a diverse range of activities and behaviors across everyday contexts.
Unlike performance-based neuropsychological tasks that measure cognitive flexibility “in the moment” during structured laboratory situations (such as the Wisconsin Card Sorting Test), the FIDL assesses trait-level flexibility as it manifests naturally across diverse real-world settings and situations (Horne et al., 2024). This ecological approach makes it particularly valuable for understanding how flexibility—or lack thereof—impacts daily functioning and quality of life.
Understanding Flexibility in Daily Life
The capacity to adjust thinking and behavior in response to environmental changes is an adaptive feature of human cognition that varies considerably between individuals and undergoes dynamic shifts across the lifespan (Anderson, 2002; Cepeda et al., 2001; Uddin, 2021). Contemporary theories increasingly view cognitive and behavioral flexibility as trait-level constructs that can be situated along a continuum, the extremes of which represent maladaptive instances of entrenched rigidity on one hand to unconstrained hyper-flexible thoughts and behaviors on the other (Armbruster et al., 2012; Uddin, 2021).
Why daily life flexibility matters:
Adaptive functioning: The ability to adjust thoughts and behaviors in response to changing demands is essential for successful navigation of everyday life challenges.
Transdiagnostic relevance: Cognitive and behavioral inflexibility is a hallmark feature across many neuropsychiatric disorders, including autism spectrum disorder, ADHD, obsessive-compulsive disorder, traumatic brain injury, and neurodegenerative diseases (Uddin, 2021).
Lifespan sensitivity: Flexibility demonstrates a U-shaped relationship with age, with lower flexibility at younger and older ages and peak flexibility in middle adulthood (Cepeda et al., 2001; Horne et al., 2024; Kupis et al., 2021).
Ecological validity: Performance on laboratory flexibility tasks does not necessarily correspond to flexible and inflexible expressions as manifested in daily life (Dang et al., 2020; Geurts et al., 2009).
Clinical utility: Understanding an individual’s flexibility profile across multiple dimensions can inform treatment planning and intervention strategies across diverse clinical populations.
Research has shown that the FIDL successfully captures natural fluctuations in flexibility across the healthy adult lifespan and provides a validated tool for detecting subtle shifts in flexibility in both health and disease (Horne et al., 2024).
Theoretical Foundation
The FIDL was developed using a deductive scale development approach aimed at capturing common themes within the flexibility literature and across neuropsychiatric diagnoses. Horne et al. (2024) recognized that existing measures of cognitive flexibility had significant limitations:
Performance-based tasks (e.g., Wisconsin Card Sorting Test, Trail Making Test) focus on isolated aspects of flexibility in structured laboratory conditions, failing to capture the full spectrum of flexible thoughts and behaviors displayed across different daily contexts (Horne et al., 2024).
Existing self-report measures are often unidimensional, disorder-specific (designed only for autism spectrum disorder), or focus narrowly on specific contexts (e.g., flexibility in response to stress), making them unsuitable for broader transdiagnostic use (Horne et al., 2024).
Ecological validity gap: Performance on neuropsychological flexibility tasks does not necessarily predict flexible behavior in real-world settings (Dang et al., 2020; Geurts et al., 2009).
The FIDL addresses these limitations by providing a multidimensional assessment that:
Captures both cognitive and behavioral manifestations of flexibility
Applies across diverse contexts and situations in daily life
Suitable for transdiagnostic use across various clinical populations
Sensitive to natural variations across the adult lifespan
The scale conceptualizes flexibility as comprising multiple interconnected dimensions, including repetitive behaviors, ability to switch mental sets, tolerance for unpredictability, reliance on routines, and rigidity of thoughts and beliefs (Horne et al., 2024).
🌟 Ecological Assessment: The FIDL bridges the gap between laboratory performance and real-world functioning by measuring how flexibility naturally expresses itself in daily life contexts, providing crucial ecological validity often missing from traditional neuropsychological measures (Horne et al., 2024).
Thoughts/Beliefs subscale: α = .76 (acceptable to good)
All subscales demonstrated moderate to strong internal consistency reliability.
Test-retest reliability:
Not yet reported in validation study. Future research needed to establish temporal stability.
Validity Evidence
Convergent validity (Horne et al., 2024):
The FIDL demonstrated significant modest correlations with the Cognitive Flexibility Inventory (CFI; Dennis & Vander Wal, 2010):
FIDL total score with CFI total: Significant moderate positive correlation
FIDL total score with CFI Control subscale: Stronger correlation than with Alternatives subscale
Individual FIDL subscales with CFI: Modest correlations in predicted directions
The moderate rather than strong correlations support that the FIDL measures related but distinct constructs compared to the CFI. The FIDL captures broader behavioral flexibility and daily life manifestations, while the CFI focuses specifically on cognitive flexibility in stressful situations (Horne et al., 2024).
Discriminant validity:
The modest correlations with CFI (rather than very high correlations) provide evidence that FIDL assesses distinct aspects of flexibility not captured by existing cognitive flexibility measures (Horne et al., 2024).
Age-related validity (Horne et al., 2024):
The FIDL demonstrated expected age-related patterns, providing evidence of construct validity:
U-shaped relationships (quadratic) with age (p < .001):
Total FIDL score
Repetition subscale
Routine subscale
Thoughts/Beliefs subscale
Peak flexibility occurred in middle age (~45-50 years), with lower flexibility in younger and older adults, consistent with prior task-switching research (Cepeda et al., 2001; Kupis et al., 2021).
Linear associations with age (p < .001):
Switching subscale: Decreased flexibility with increasing age
Predictability/Control subscale: Decreased flexibility with increasing age
These differential age patterns across subscales provide evidence that the FIDL captures distinct dimensions of flexibility with different developmental trajectories.
Factor Structure Validation
Five clearly differentiated factors emerged, each representing distinct manifestations of flexibility:
Factors capture both cognitive (Switching, Thoughts/Beliefs) and behavioral (Repetition, Routine) aspects
Clear factor structure supports multidimensional conceptualization of flexibility
No excessive cross-loadings, supporting discriminant validity of subscales
Sensitivity to Lifespan Changes
The FIDL’s ability to detect U-shaped and linear age-related patterns demonstrates its sensitivity to natural fluctuations in flexibility across adulthood (Horne et al., 2024). This is a unique strength, as most existing measures have not been validated across the full adult lifespan or shown to be sensitive to age-related variations.
Limitations and Future Directions
Acknowledged limitations (Horne et al., 2024):
Single sample validation: Factor structure should be confirmed via CFA in independent sample
Healthy adults only: Validation needed in clinical populations with known flexibility deficits
Test-retest reliability: Temporal stability not yet established
Cultural validation: Validated only in United States residents
Concurrent clinical validity: Associations with functional outcomes and disorder severity not yet examined
Recommended future research:
Confirmatory factor analysis in independent sample
Validation in clinical populations (ASD, ADHD, OCD, TBI, neurodegenerative diseases)
Establishment of clinical cutoffs and norms
Test-retest reliability studies
Cross-cultural validation
Investigation of relationships with functional outcomes
Sensitivity to treatment effects
Comparison with performance-based flexibility measures
Usage Guidelines and Applications
Primary Research Applications
Clinical neuropsychology – Transdiagnostic assessment across diverse patient populations
Lifespan developmental research – Tracking flexibility changes from young to older adulthood
Intervention research – Measuring treatment effects on multidimensional flexibility
Neuropsychiatric research – Characterizing flexibility profiles across disorders
Cognitive aging studies – Understanding age-related changes in daily life flexibility
Occupational psychology – Assessing workplace adaptability and functioning
Rehabilitation research – Monitoring recovery of flexibility after brain injury
Clinical Assessment Applications
Diagnostic evaluation:
Characterize flexibility deficits across multiple dimensions
Identify specific areas of inflexibility (e.g., behavioral vs. cognitive)
Copyright and Usage Responsibility: Check that you have the proper rights and permissions to use this assessment tool in your research. This may include purchasing appropriate licenses, obtaining permissions from authors/copyright holders, or ensuring your usage falls within fair use guidelines.
The Flexibility in Daily Life scale was developed for research and clinical use. Researchers should contact the authors regarding proper usage and attribution.
Proper Attribution: When using or referencing this scale, cite the original development:
Horne, K., Chen, T., & Irish, M. (2024). Development of the Flexibility in Daily Life scale to measure multidimensional cognitive and behavioural flexibility in health and disease. British Journal of Clinical Psychology, 64(2), 315-329. https://doi.org/10.1111/bjc.12505
Horne, K., Chen, T., & Irish, M. (2024). Development of the Flexibility in Daily Life scale to measure multidimensional cognitive and behavioural flexibility in health and disease. British Journal of Clinical Psychology, 64(2), 315-329. https://doi.org/10.1111/bjc.12505
Theoretical Foundation:
Anderson, P. (2002). Assessment and development of executive function (EF) during childhood. Child Neuropsychology, 8(2), 71-82.
Armbruster, D. J. N., Ueltzhöffer, K., Basten, U., & Fiebach, C. J. (2012). Prefrontal cortical mechanisms underlying individual differences in cognitive flexibility and stability. Journal of Cognitive Neuroscience, 24(12), 2385-2399.
Cepeda, N. J., Kramer, A. F., & Gonzalez de Sather, J. C. M. (2001). Changes in executive control across the life span: Examination of task-switching performance. Developmental Psychology, 37(5), 715-730.
Uddin, L. Q. (2021). Cognitive and behavioural flexibility: Neural mechanisms and clinical considerations. Nature Reviews Neuroscience, 22(3), 167-179.
Convergent Validity:
Dennis, J. P., & Vander Wal, J. S. (2010). The Cognitive Flexibility Inventory: Instrument development and estimates of reliability and validity. Cognitive Therapy and Research, 34(3), 241-253.
Ecological Validity:
Dang, L. C., Castrellon, J. J., Perkins, S. F., Le, N. T., Cowan, R. L., Zald, D. H., & Samanez-Larkin, G. R. (2020). Reduced effects of age on dopamine D2 receptor levels in physically active adults. NeuroImage, 148, 116-122.
Geurts, H. M., Corbett, B., & Solomon, M. (2009). The paradox of cognitive flexibility in autism. Trends in Cognitive Sciences, 13(2), 74-82.
Age-Related Research:
Kupis, L., Goodman, Z. T., Kornfeld, S., Hoang, S., Romero, C., Dirks, B., Dehoney, J., Chang, C., & Uddin, L. Q. (2021). Brain dynamics underlying cognitive flexibility across the lifespan. Cerebral Cortex, 31(11), 5263-5274.
Related Measures:
Bodfish, J. W., Symons, F. J., Parker, D. E., & Lewis, M. H. (2000). Varieties of repetitive behavior in autism: Comparisons to mental retardation. Journal of Autism and Developmental Disorders, 30(3), 237-243.
Strang, J. F., Kenworthy, L., Daniolos, P., Case, L., Wills, M. C., Martin, A., & Wallace, G. L. (2012). Depression and anxiety symptoms in children and adolescents with autism spectrum disorders without intellectual disability. Research in Autism Spectrum Disorders, 6(1), 406-412.
Uljarević, M., Baranek, G., Vivanti, G., Hedley, D., Hudry, K., & Lane, A. (2023). Heterogeneity of restricted and repetitive behaviors in autism spectrum disorder. Journal of Autism and Developmental Disorders, 53(9), 3350-3368.
Clinical Applications:
Bozeat, S., Gregory, C. A., Ralph, M. A. L., & Hodges, J. R. (2000). Which neuropsychiatric and behavioural features distinguish frontal and temporal variants of frontotemporal dementia from Alzheimer’s disease? Journal of Neurology, Neurosurgery & Psychiatry, 69(2), 178-186.
Dajani, D. R., Llabre, M. M., Nebel, M. B., Mostofsky, S. H., & Uddin, L. Q. (2016). Heterogeneity of executive functions among comorbid neurodevelopmental disorders. Scientific Reports, 6, 36566.
Robbins, T. W., & Cools, R. (2014). Cognitive deficits in Parkinson’s disease: A cognitive neuroscience perspective. Movement Disorders, 29(5), 597-607.
Platypuses thriving in water and on land — embodying adaptability, versatility, and psychological flexibility measured by the FIDL (Flexibility in Daily Life Scale)
Frequently Asked Questions
What does the FIDL measure?
The FIDL measures cognitive and behavioral flexibility as it naturally manifests in daily life across five dimensions: repetitive behaviors, task/mental set switching ability, tolerance for unpredictability, reliance on routines, and rigidity of thoughts and beliefs. Unlike laboratory tasks, it assesses trait-level flexibility across diverse real-world contexts.
How long does the FIDL take to complete?
The FIDL takes approximately 10-15 minutes to complete. It consists of 21 items rated on a 5-point Likert scale, making it brief and practical for both clinical and research applications.
Is the FIDL free to use?
The FIDL was developed for research and clinical use. Researchers should contact the authors regarding proper usage and attribution. When using the scale, proper citation of the original development article (Horne, Chen, & Irish, 2024) is required.
How is the FIDL scored?
After reverse scoring positively worded items, sum items for each of the five subscales and calculate a total score (range: 21-105). Higher scores indicate greater inflexibility/rigidity, while lower scores indicate greater flexibility. Both total and subscale scores can be interpreted.
What's the difference between FIDL and the Cognitive Flexibility Inventory?
The FIDL assesses multidimensional cognitive and behavioral flexibility across diverse daily life contexts with five subscales, while the CFI focuses specifically on cognitive flexibility in stressful situations. The FIDL provides broader ecological assessment of both cognitive and behavioral manifestations, whereas the CFI emphasizes cognitive responses to stress.
How reliable is the FIDL?
The FIDL demonstrates good to excellent internal consistency with total score α = .85 and subscale alphas ranging from .72 to .79. All subscales show acceptable to good reliability. However, test-retest reliability has not yet been established and requires future research.