Skip to content

Assembly

Cognitive

Cognitive impairment is a comorbidity that occurs in response to a complex interplay of systemic factors, resulting in heightened vulnerability to adverse health outcomes.1  Deficits in cognition, specifically in attention, memory, and executive function, are highly prevalent in chronic lung disease, with a prevalence between 25% to 75% among COPD patients.1 Cognitive dysfunction is gaining increasing recognition in chronic lung disease as it can impair an individual’s ability to manage complex therapeutic regimens, increases the risk of hospitalizations, and is associated with worse health-related quality of life.2 Furthermore, symptoms such as dyspnea can impose an additional "cognitive load", limiting functional performance during activities of daily living.3  Unfortunately, many have had limited use in PR.

No single best method currently exists to assess the full spectrum of cognitive function in this population. Shorter screening tools and digital batteries are increasingly utilized to detect deficits in processing speed, psychomotor sequencing, and working memory.
The following instruments are described:

We thank the following who collated this material: Alessandra Adami PhD, Department of Kinesiology, College of Health Sciences, University of Rhode Island, Kingston, RI, US; Peter Rassam, University Health Network, Toronto, Canada; Darlene Reid, PhD University of Toronto, Toronto, Canada; Dmitry Rozenberg, MD, PhD (Lead) University Health Network, Temerty Faculty of Medicine, University of Toronto, Toronto, Canada; W. Ali A. Salman Al-Timimi, University Health Network, Toronto, Canada; Suzanne Lareau, MS, RN (Co-Ed) (University of Colorado, Denver, US) Clarice Tang PhD (Co-Ed), Victoria University, Melbourne, Australia.

References:

  1. Ranzini L, et al. Front Psychol 2020; 11:337.
  2. Chang SS, et al. J Am Geriatr Soc 2012; 60:1839-1846.3 Rozenberg D, et al. Chest 2024; 166:721-732.

 

PRA OUTCOMES

Wechsler Adult Intelligence Scale - Digit Span Test

 

Description

Name of QuestionnaireWechsler Adult Intelligence Scale (WAIS) – Digit Span Test
Abbreviation/Alternate NameWAIS-IV Digit Span; WMI (Working Memory Index)
Description:Cognitive test (part of WAIS) of working memory. 1
DeveloperDavid Wechsler (Original, 1955). 1 Pearson Clinical (Current). 
E-mailhttps://www.pearsonassessments.com/en-us/Store/Professional-Assessments/Cognition-%26-Neuro/Wechsler-Adult-Intelligence-Scale-%7C-Fourth-Edition/p/100000392 (Publisher)
CostPart of WAIS-IV Kit. Record forms sold separately (~$200 for 25).
License requiredCopyright © 2008 NCS Pearson, Inc.
Self-or rater-administeredRater-administered
Time to complete5–10 minutes
Number of itemsPairs of trials increasing in length from 2 to 9 digits.
Domains & categories (#)3 (WAIS-IV version).
Name of domains/ categories

Digit Span Forward (DSF), Digit Span Backward (DSB),

Digit Span Sequencing (DSS).2 

Scaling of items1 point/correct response.3 
ScoringTotal Raw Score: Sum of correct trials for Forward, Backward, and Sequencing (Max 48 in WAIS-IV).3 
Test-retest/ reproducibility Test-rest reliability in healthy adults (0.70 to 0.80).3 
Validity DSS may potentially be a more sensitive measure of working memory capacity than DSF.2 
Responsiveness to PR 

DSF: pre-post mean D = 0.06 (in male COPD patients) and 0.79 (in female COPD patients).

DSB: pre-post mean D = - 0.36 (in male COPD patients) and 0.67 (in female COPD patients) (p > 0.05).4 

MIDNot established for pulmonary diseases.
LanguagesAvailable in several languages.
References

1. Wechsler, David (1939). The Measurement of Adult Intelligence. Baltimore (MD): Williams & Witkins.

2. Egeland J et al. Appl Neuropsychol Adult. 2026; 33(1); 65-72.

3. Stafford C & Bennett R. Digit Span. In: Clinical Integration of Neuropsychological Test Results. 1 st ed. CRC Press. 2024.

4. Emery CF et al. Chest. 1991;100:613-7.

Date of most recent updates January 2026

 

PRA OUTCOMES

Wechsler Adult Intelligence Scale - Digit Symbol 

 

Description

Name of QuestionnaireWechsler Adult Intelligence Scale (WAIS)© - Digit Symbol
Abbreviation/Alternate NameWAIS-IV Coding; Digit Symbol Substitution Test (DSST); Digit Symbol
Description:A test that assesses psychomotor speed and visual-motor coordination. 1
DeveloperDavid Wechsler (Original, 1955) 1 Pearson Clinical (Current). 
E-mailhttps://www.pearsonassessments.com/en-us/Store/Professional-Assessments/Cognition-%26-Neuro/Wechsler-Adult-Intelligence-Scale-%7C-Fourth-Edition/p/100000392 (Publisher)
CostPart of WAIS-IV Kit. Record forms sold separately (~$200 for 25).
License requiredCopyright © 2008 NCS Pearson, Inc.
Self-or rater-administeredRater-administered.
Time to complete90 to 120 seconds.
Number of items135 items (WAIS-IV version).
Domains & categories (#)1
Name of domains/categoriesCoding (Part of Processing Speed Subset)
Scaling of itemsNumbers (1–9) are paired with unique symbols. Participants match symbols to their corresponding number within the time limit.21 point for each correctly drawn symbol within the time limit. 
ScoringRaw score (0–135) converted to Scaled Score (1-19). 2
Test-retest/ reproducibility Test-retest reliability > 0.80 in clinical adult populations2 
Validity Coding (WAIS-IV) shown to have moderate-to-strong correlation with other processing speed subtests.2 
Responsiveness to PR Pre-post mean D = 5.62 male COPD patients and 6.61 female (p < 0.05).3 
MIDNot established for pulmonary diseases.
LanguagesAvailable in several languages.
References

1. Wechsler, David (1939). The Measurement of Adult Intelligence. Baltimore (MD): Williams & Witkins.

2. Arnold M. Coding. In: Clinical Integration of Neuropsychological Test Results. 1 st ed. CRC Press. 2024.

3. Emery CF et al. Chest. 1991;100:613-7.

Date of most recent updatesJanuary 2026

 

PRA OUTCOMES

Digit Vigilance Test

 

Description

Name of QuestionnaireDigit Vigilance Test
Abbreviation/Alternate NameDVT; Lewis DVT
Description:Assesses sustained attention (vigilance) and psychomotor speed by asking participants to scan two pages of random numbers and cross out all 6s and 9s as quickly and accurately as possible. 1
DeveloperRonald F. Lewis (1995).
E-mailhttps://www.parinc.com/products/DVT (Publisher)
Cost~$200 USD for a kit (Manual + 25 Test Booklets).
License requiredCopyright © 1995 Psychological Assessment Resources (PAR).
Self-or rater-administeredRater-administered.
Time to complete10 minutes.
Number of items59 rows of digits
Domains & categories (#)2
Name of domains/ categoriesTotal Time (Psychomotor Speed), Accuracy (Errors of Omission & Commission)
Scaling of itemsRaw values (errors and total time) compared to normative data for age, education and socioeconomic status 
ScoringTotal Time: Seconds to complete. Errors: Count of missed targets (Omissions) or wrong targets (Commissions). 2
Test-retest/ reproducibility Test-retest reliability in young adults r= .91.
Validity DVT total errors correlate with Discriminant Reaction Time Test (r = .503); total time =ns. 2
Responsiveness to PR Pre-post mean D = 2.6 in COPD patients. 3
MIDNot established for pulmonary diseases.
LanguagesAvailable in several languages.
References

1. Lewis RF. Digit vigilance test. Odessa, FL: Psychological Assessment Resources; 1995.

2. Kelland DZ & Lewis RF. Arch Clin Neuropsychol. 1996;11: 339-344.

3. Emery CF et al. Health Psychol. 1998;17:232-240.

Date of most recent updatesJanuary 2026

 

PRA OUTCOMES

Finger Tapping Test

 

Description

Name of QuestionnaireFinger Tapping Test
Abbreviation/Alternate NameFTT; Finger Oscillation Test; Halstead Finger Tapping Test
Description:Measure of psychomotor speed and motor function by index finger tapping on an apparatus as rapidly as possible for 10-second intervals.
DeveloperHalstead (1947); Reitan (1969).
E-mailhttps://neuropsych.com/product/finger-tapping-test-adults-older-children/ 
Cost~$425 USD
License requiredNo
Self-or rater-administeredRater-administered
Time to complete5-15 minutes
Number of items5 consecutive 10-second trials per hand (Total 10 recorded trials).
Domains & categories (#)2
Name of domains/ categoriesDominant and non-dominant hand motor speed.
Scaling of itemsCount of taps per 10-second interval. 2
ScoringAverage number of taps across 5 consecutive trials for each hand . 2
Test-retest/ reproducibility

Test-retest (young healthy adults):

  • Dominant hand (0.80)
  • Non-dominant hand (0.82) 3
Validity Correlates with Purdue peg placement in adults (r = 0.78). 2
Responsiveness to PR 

Dominant hand: pre-post D = 2.05 (in male COPD patients) and 3.61 (in female COPD patients)

Non-dominant hand: pre-post D = 1.45 (males with COPD) and 0.22 (in females) p < 0.05. 4

MIDNot established for pulmonary diseases.
LanguagesAvailable in several languages.
References

1. Cousins MS et al. Pharm Biochem Behm 1998; 59:445-449.

2. Castro K. Finger Tapping Test (FTT). In: Clinical Integration of Neuropsychological Test Results. 1 st ed. CRC Press. 2024.

3. Morrison MW et al. Percept Mot Skills. 1979; 48:139-142.

4. Emery CF et al. Chest .1991; 100:613-7.

Date of most recent updatesJanuary 2026

 

PRA OUTCOMES

Mini-Mental State Examination

 

Description

Name of QuestionnaireMini-Mental State Examination
Abbreviation/Alternate NameMMSE; MMSE-2 (2 nd edition); Folstein Test
Description:Screening tool for cognitive impairment.
DeveloperMF Folstein 1
E-mailcopyright@parinc.com 
Cost$119.00 (50 Test Forms), PAR, Inc.
License requiredCopyright https://www.parinc.com/products/MMSE
Self-or rater-administeredRater-administered
Time to complete10-15 minutes; 5 minutes to score.
Number of items11
Domains & categories (#)6
Name of domains/ categoriesOrientation, Registration, Attention & Calculation, Recall, Language, and Visuospatial.
Scaling of itemsOrientation (0-10), Registration (0-3), Attention and Calculation (0-5), Recall (0-3), Language (0-8), Visuospatial (0-1)
Scoring

Higher score reflects better cognitive function (0-30)

· 24-30 No impairment

· 18-23 Mild

· 0-17 Severe 2

Test-retest/ reproducibility 

Internal consistency: Cronbach’s a = 0.68-0.96

Test-Retest Reliability: r = 0.68 to 0.95 2

Validity Lower validity than MoCA for detecting mild cognitive impairment in COPD. 3
Responsiveness to PR 

Mean change using standardized MMSE in COPD:

- without cognitive impairment: D 0.5 ± 1.2 (p <0.05). 4

- with cognitive impairment: D 0.7 ± 1.1 (p <0.05). 4

MIDNot available in pulmonary diseases.
Languages>70 Translations (https://www.parinc.com/products/MMSE)
References

1. Folstein MF et al. J Psychiatr Res. 1975; 12:189-98.

2. Tombaugh TN & McIntyre NJ. J Am Geriatr Soc. 1992; 40:922-35.

3. Villeneuve S et al. Chest. 2012; 142:1516-1523.

4. Andrianopoulos V et al. Respir Med. 2021; 185:106478.

Date of most recent changes January 2026

 

PRA OUTCOMES

Montreal Cognitive Assessment

 

Description

Name of QuestionnaireMontreal Cognitive Assessment 1
Abbreviation/Alternate NameMoCA©
Description:Early detection of mild cognitive impairment (MCI) 
DeveloperZiad Nasreddine https://mocacognition.com 
E-mailinfo@mocacognition.com 
CostTraining certification US $150.00 if not students, faculty members, academic researchers and publicly operated healthcare institutions. Free after certification/signing disclaimer.
License requiredTraining & certification mandatory for “all clinicians, researchers, health professionals, and workers administering MoCA for clinical or research purposes”.
Self-or rater-administeredSelf and trained by interviewer in person or by telephone.2 
Time to complete5 min telephone to 15 min (paper version).
Number of items30
Domains & categories (#)6
Name of domains/ categoriesAttention, orientation, language, verbal memory, visuospatial, and executive function.
Scaling of items0 to 6 points
Scoring0-30 (high scores more favorable). Total score and subscores on each of 6 domains: >26; normal; 18–25 mild; 10–17 moderate; <10 severe cognitive impairment 1
Test-retest/ reproducibility 
  • Test-retest r=0.92, p<0.001 1
  • Internal consistency Cronbach a= 0.83 1
Validity Content validity vs. MMSE 1,2
Responsiveness to PR 

· 3 months post PR, Pre 22, post 25 p<.01 3

· Those with mild CI and ECOPD 6 wk PR (Δ1.6 ± 2.4, p = 0.004), no change in those without CI 4

MIDNot available in pulmonary disease
Languages>100 (https://mocacognition.com)
References

1. Nasreddine et. al. J Am Geriatr Soc 2005; 53: 695-699.

2. Eastus et al. Front Rehabil Sci 2022; 3: 987356.

3. Bonnevie et. al. Int J Chronic Obstruct Pulmon Dis 2020; 15: 1111-1121

4. Frances et. al. Respir Med 2021; 176: 106249.

Date of most recent changes January 2026

 

PRA OUTCOMES

Rey Auditory Verbal Learning Test

 

Description

Name of QuestionnaireRey Auditory Verbal Learning Test
Abbreviation/Alternate NameRAVLT™; Rey AVLT; AVLT
Description:Assesses verbal learning, immediate recall, delayed recall, and recognition memory. Evaluates episodic memory and susceptibility to interference. 1,2,3 
DeveloperAndré Rey (Original, 1958). Adapted by Michael Schmidt (1996).
E-mailhttps://www.wpspublish.com/ravlt-rey-auditory-verbal-learning-test (Publisher)
CostFees apply for commercial kits (manuals/forms). Word lists often found in public domain for research, but standardized norms/forms require purchase.
License requiredCopyright © 1996 by Western Psychological Services.
Self-or rater-administeredRater-administered.
Time to complete10–15 minutes (active testing). Total time ~45 mins including delay interval.4 
Number of items30 words total (15 words in List A + 15 words in List B).
Domains & categories (#)5
Name of domains/ categoriesLearning (List A Trials 1–5); Interference (List B); Immediate Recall (List A Trial 6); Delayed Recall (List A Trial 7); Recognition (List A).
Scaling of items0-15/trial
ScoringNumber of correct words.4,5 
Test-retest/ reproducibility

Test-retest total learning recall (Trials 1-5, r= 0.68).

Internal consistency Cronbach a = 0.80 in young healthy adults.6 

Validity 

RAVLT learning (i.e., sum of first 5 trials) correlates with Benton Visual Retention Test (BVRT) immediate recall (r = 0.44, p < 0.01).

RAVLT delayed recall correlates with BVRT delayed recall (r = 0.39, p < 0.05).6 

Responsiveness to PR 

3-months PR:

RAVLT sum of first 5 trials: = 6.23, 95% CI [3.24, 9.23]

RAVLT immediate recall: = 1.14, 95% CI [0.34, 1.94]

RAVLT delayed recall: = 1.11, 95% CI [0.16, 2.07]7 

MIDNot established for pulmonary diseases.
LanguagesAvailable in several languages.
References

1. Rosenberg SJ et al. J Clin Psychol. 1984;40:785-787.

2. Loring DW et al. J Int Neuropsychol Soc. 2023;29:397-405.

3. McMinn et al. Clin Neuropsychol. 1988;2:67-87.

4. UDS Instructions Form C2T. Univ of Washington; 2025;30-31.

5. Stricker et al. J Int Neuropsychol Soc. 2020;27;211-226.

6. Magalhaes SDS et al. Clin Neuropsych. 2012;9:129-137.

7. Pereira ED et al. Lung. 2011;189:279-285.

Date of most recent updatesJanuary 2026

 

PRA OUTCOMES

Trail Making Test

 

Description

Name of QuestionnaireTrail Making Test 1
Abbreviation/Alternate NameTMT
Description:A test to assess cognitive function (psychomotor speed, visual attention, working memory, executive function). Trail A and B; are part of the Halstead-Reitan Neuropsychological Battery.
DeveloperJohn E. Partington & Russell G. Leiter 1
E-mailhttps://eatspeakthink.com/wp-content/uploads/2018/06/IowaTrailMaking.pdf
CostFree.
License requiredNo
Self-or rater-administeredRater-administered.
Time to complete5 to 10 minutes.
Number of itemsPart A consists of connecting 25 numbered circles (1 to 25) in ascending order; Part B 25 circles alternating numbers and letters (1 to 13, A to L).
Domains & categories (#)Two.
Name of domains/categoriesParts A & Part B.
Scaling of itemsIn seconds
ScoringNumber of seconds to complete Part A and Part B. Higher scores indicate greater cognitive impairment. 1
Test-retest/reproducibility

Test-retest reliability:

  • Part A: r = 0.46 (young adult males)2, 0.78 (cerebrovascular disease)2, and

0.69 (neuropsychiatric patients). 3

  • Part B: r = 0.44 (young adult males)2, 0.67 (cerebrovascular disease)2, and

0.66 (neuropsychiatric patients). 3

Validity Construct validity: Part A (visuoperceptual abilities) and Part B (working memory and task-switching).
Responsiveness to PR 

· Part A: pre-post mean D = -2.17 (in male COPD patients) and -4.02 (in female COPD patients).

· Part B: pre-post mean D = -33.89 (in male COPD patients) and -40.4 (in female COPD patients) (p < 0.05). 5

MIDNot available for pulmonary diseases.
LanguagesAvailable in several languages.
References

1. Reitan RM.. Percept Mot Skills . 1958;8:271-276..

2. Matarazzo JD et al. J Nerv Ment Dis. 1974;158:37-49.

3. Goldstein G et al. Clinical Neuropsychol.1989;3:265-272.

4. Sanchez-Cubillo I et al. J Int Neuropsychol Soc. 2009;15:438-50.

5. Emery CF et al. Chest. 1991;100:613-7.

Date of most recent changes January 2026