The efficacy of a task model approach to ADL rehabilitation in stroke apraxia and action disorganisation syndrome: A randomised controlled trial

Jo Howe, Winnie Chua, Emily Sumner, Bogna Drozdowska, Rosanna Laverick, Rachel L Bevins, Emilie Jean-Baptiste, Martin Russell, Pia Rotshtein, Alan M Wing, Jo Howe, Winnie Chua, Emily Sumner, Bogna Drozdowska, Rosanna Laverick, Rachel L Bevins, Emilie Jean-Baptiste, Martin Russell, Pia Rotshtein, Alan M Wing

Abstract

Background: Apraxia and action disorganization syndrome (AADS) after stroke can disrupt activities of daily living (ADL). Occupational therapy has been effective in improving ADL performance, however, inclusion of multiple tasks means it is unclear which therapy elements contribute to improvement. We evaluated the efficacy of a task model approach to ADL rehabilitation, comparing training in making a cup of tea with a stepping training control condition.

Methods: Of the 29 stroke survivors with AADS who participated in this cross-over randomized controlled feasibility trial, 25 were included in analysis [44% females; mean(SD) age = 71.1(7.8) years; years post-stroke = 4.6(3.3)]. Participants attended five 1-hour weekly tea making training sessions in which progress was monitored and feedback given using a computer-based system which implemented a Markov Decision Process (MDP) task model. In a control condition, participants received five 1-hour weekly stepping sessions.

Results: Compared to stepping training, tea making training reduced errors across 4 different tea types. The time taken to make a cup of tea was reduced so the improvement in accuracy was not due to a speed-accuracy trade-off. No improvement linked to tea making training was evident in a complex tea preparation task (making two different cups of tea simultaneously), indicating a lack of generalisation in the training.

Conclusions: The clearly specified but flexible training protocol, together with information on the distribution of errors, provide pointers for further refinement of task model approaches to ADL rehabilitation. It is recommended that the approach be tested under errorless learning conditions with more impaired patients in future research.

Trial registration: Retrospectively registered at ClinicalTrials.gov on 5th August 2019 [NCT04044911] https://ichgcp.net/clinical-trials-registry/NCT04044911?term=Cogwatch&rank=1.

Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1. Consort diagram showing the flow…
Fig 1. Consort diagram showing the flow of participants through the study.
Fig 2. Object layout for simple tea…
Fig 2. Object layout for simple tea at assessment.
(a) Simple and (b) Complex Tea Layout Mat to scale (80x50cm); kettle (15cm diameter) bowls & water jug (12.8cm), cups, milk and coffee (8cm), cutlery (13.7–17.7cm), sweetener (4.5cm). Coffee was used as a distractor.
Fig 3. CogWatch system setup.
Fig 3. CogWatch system setup.
a) As the patient completes tea-making with the items on the table layout, cues are presented on the “patient display” (foreground) when an error is detected (in this case non-recoverable). The healthcare professional monitors task progression via the “clinician display” (background). b) Each correct step is acknowledged by the system by displaying a visual reminder of the completed sub-action at the top of the patient display. Here, the patient has completed “Add water from jug to kettle”, “Boil water”, “Add teabag to cup”, “Add sugar”, “Add milk” and is performing the sub-action of “Add boiled water to cup”. We acknowledge The Stroke Association, UK, as the source of this figure. The individuals in this figure have given written informed consent (as outlined in the PLOS consent form) to publish their image.
Fig 4. Mapping of actions and errors…
Fig 4. Mapping of actions and errors to neuropsychological classification.
From left to right are the sub-actions which are performed during simple tea making, action errors which may result during performance of the sub-actions, and their relation to the neuropsychological error categories which were used for analysis. In addition to errors which were trained by the Cogwatch subsystem, 4 additional errors were identified during the assessment (in boxes with broken line borders).
Fig 5. Tea making performance.
Fig 5. Tea making performance.
(a) error (b) time taken for the two patient groups (Group 1: Baseline (1), Post-training (2), Post-control (3), Follow-up (4); Group 2: Baseline (1), Post-control (2), Post-training (3), Follow-up (4)). Tea making change scores (c) Recoverable and nonrecoverable errors (d) time as a function of condition. Experimental, control and follow-up scores were calculated 1–2, 2–3, 2–4 (where experimental, control and follow-up were calculated as Group1) and 2–3,1–2, 3–4 (Group 2). Statistically significant contrasts are shown across the top of (c, d).
Fig 6. Error changes.
Fig 6. Error changes.
Number of three types of non-recoverable (addition N-ADD, object substitution N-OSUB, kettle error N-KET) and six types of recoverable errors (addition N-ADD, object substitution N-OSUB, kettle error N-KET) before (dark shade bars) and after tea-making training (light shade bars). Note that only data from complete cases (n = 22) are included in this figure as error type data were not imputed.
Fig 7. Error types.
Fig 7. Error types.
Relative proportions of the three types of non-recoverable errors (addition N-ADD, object substitution N-OSUB, kettle error N-KET in shades of green) and six types of recoverable errors (continuous perseveration R-CP, execution R-EX, recurrent perseveration R-RP, sequence R-SEQ, quantity underestimation R-QU, step omission R-SOM in shades of blue) pre and post-tea making training. Note that no non-recoverable step omission errors occurred during the pre and post-tea making sessions.
Fig 8. Complex tea making.
Fig 8. Complex tea making.
(a) Proportion of complex tea making errors as a function of training condition. (b) Mean change in complex tea making errors across contrasts.

References

    1. Dobkin BH. Clinical practice. Rehabilitation after stroke. N Engl J Med. 2005;352(16):1677–84. doi: 10.1056/NEJMcp043511
    1. Goldenberg G. Apraxia: the cognitive side of motor control 2013.
    1. Humphreys GW, Forde EME. Disordered action schema and action disorganisation syndrome. Cogn Neuropsychol. 1998;15(6–8):771–811.
    1. Buxbaum LJ, Randerath J. Limb apraxia and the left parietal lobe. Handb Clin Neurol. 2018;151:349–63. doi: 10.1016/B978-0-444-63622-5.00017-6
    1. Watson CE, Buxbaum LJ. A distributed network critical for selecting among tool-directed actions. Cortex. 2015;65:65–82. doi: 10.1016/j.cortex.2015.01.007
    1. Hanna-Pladdy B, Daniels SK, Fieselman MA, Thompson K, Vasterling JJ, Heilman KM, et al.. Praxis lateralization: errors in right and left hemisphere stroke. Cortex. 2001;37(2):219–30. doi: 10.1016/s0010-9452(08)70569-0
    1. Flores-Medina Y, Chavez-Oliveros M, Medina LD, Rodriguez-Agudelo Y, Solis-Vivanco R. Brain lateralization of complex movement: neuropsychological evidence from unilateral stroke. Brain Cogn. 2014;84(1):164–9. doi: 10.1016/j.bandc.2013.11.010
    1. Ballinger C, Ashburn A, Low J, Roderick P. Unpacking the black box of therapy—a pilot study to describe occupational therapy and physiotherapy interventions for people with stroke. Clin Rehabil. 1999;13(4):301–9. doi: 10.1191/026921599673198490
    1. De Wit L, Putman K, Lincoln N, Baert I, Berman P, Beyens H, et al.. Stroke rehabilitation in Europe: what do physiotherapists and occupational therapists actually do? Stroke. 2006;37(6):1483–9. doi: 10.1161/01.STR.0000221709.23293.c2
    1. Intercollegiate Stroke Working Party. National clinical guideline for stroke. 2016.
    1. Alashram AR, Annino G, Aldajah S, Raju M, Padua E. Rehabilitation of limb apraxia in patients following stroke: a systematic review. Appl Neuropsychol Adult. 2021:1–11. doi: 10.1080/23279095.2021.1900188
    1. Worthington A. Treatments and technologies in the rehabilitation of apraxia and action disorganisation syndrome: A review. NeuroRehabilitation. 2016;39(1):163–74. doi: 10.3233/NRE-161348
    1. Aguilar-Ferrandiz ME, Toledano-Moreno S, Garcia-Rios MC, Tapia-Haro RM, Barrero-Hernandez FJ, Casas-Barragan A, et al.. Effectiveness of a Functional Rehabilitation Program for Upper Limb Apraxia in Poststroke Patients: A Randomized Controlled Trial. Arch Phys Med Rehabil. 2021;102(5):940–50. doi: 10.1016/j.apmr.2020.12.015
    1. Sackley CM, Walker MF, Burton CR, Watkins CL, Mant J, Roalfe AK, et al.. An occupational therapy intervention for residents with stroke related disabilities in UK care homes (OTCH): cluster randomised controlled trial. BMJ. 2015;350:h468. doi: 10.1136/bmj.h468
    1. Legg L, Drummond A, Leonardi-Bee J, Gladman JR, Corr S, Donkervoort M, et al.. Occupational therapy for patients with problems in personal activities of daily living after stroke: systematic review of randomised trials. BMJ. 2007;335(7626):922. doi: 10.1136/bmj.39343.466863.55
    1. Walker MF, Sunderland A, Fletcher-Smith J, Drummond A, Logan P, Edmans JA, et al.. The DRESS trial: a feasibility randomized controlled trial of a neuropsychological approach to dressing therapy for stroke inpatients. Clin Rehabil. 2012;26(8):675–85. doi: 10.1177/0269215511431089
    1. Creighton C. The origin and evolution of activity analysis. Am J Occup Ther. 1992;46(1):45–8. doi: 10.5014/ajot.46.1.45
    1. Hughes CM, Baber C, Bienkiewicz M, Worthington A, Hazell A, Hermsdorfer J. The application of SHERPA (Systematic Human Error Reduction and Prediction Approach) in the development of compensatory cognitive rehabilitation strategies for stroke patients with left and right brain damage. Ergonomics. 2015;58(1):75–95. doi: 10.1080/00140139.2014.957735
    1. Jean-Baptiste EMD, Nabiei R, Parekh M, Fringi E, Drozdowska B, Baber C, et al.. Intelligent Assistive System Using Real-Time Action Recognition for Stroke Survivors. 2014 Ieee International Conference on Healthcare Informatics (Ichi). 2014:39–44.
    1. Goldenberg G, Daumuller M, Hagmann S. Assessment and therapy of complex activities of daily living in apraxia. Neuropsychol Rehabil. 2001;11(2):147–69.
    1. Cappa SF, Benke T, Clarke S, Rossi B, Stemmer B, van Heugten CM, et al.. EFNS guidelines on cognitive rehabilitation: report of an EFNS task force. Eur J Neurol. 2005;12(9):665–80. doi: 10.1111/j.1468-1331.2005.01330.x
    1. Wilson BA, Baddeley A, Evans J, Shiel A. Errorless Learning in the Rehabilitation of Memory-Impaired People. Neuropsychol Rehabil. 1994;4(3):307–26.
    1. Hazell A, Worthington A, Walton C. Report on healthcare professionals and caregivers requirements II. 2013.
    1. Rusted J, Sheppard L. Action-based memory in Alzheimer’s disease: a longitudinal look at tea making. Neurocase. 2002;8(1–2):111–26. doi: 10.1093/neucas/8.1.111
    1. Jean-Baptiste EMD, Russell M, Howe J, Rotshtein P. Intelligent prompting system to assist stroke survivors. J Amb Intel Smart En. 2017;9(6):707–23.
    1. Thaut MH, Abiru M. Rhythmic Auditory Stimulation in Rehabilitation of Movement Disorders: A Review of Current Research. Music Percept. 2010;27(4):263–9.
    1. Thaut AH, Leins AK, Rice RR, Argstatter H, Kenyon GP, McIntosh GC, et al.. Rhythmic auditory stimulation improves gait more than NDT/Bobath training in near-ambulatory patients early poststroke: A single-blind, randomized trial. Neurorehab Neural Re. 2007;21(5):455–9. doi: 10.1177/1545968307300523
    1. Wright RL, Brownless SB, Pratt D, Sackley CM, Wing AM. Stepping to the Beat: Feasibility and Potential Efficacy of a Home-Based Auditory-Cued Step Training Program in Chronic Stroke. Front Neurol. 2017;8:412. doi: 10.3389/fneur.2017.00412
    1. Humphreys GW. BCoS brain behaviour analysis. Hove: Psychology Press; 2012.
    1. Bienkiewicz MM, Brandi ML, Goldenberg G, Hughes CM, Hermsdorfer J. The tool in the brain: apraxia in ADL. Behavioral and neurological correlates of apraxia in daily living. Front Psychol. 2014;5:353. doi: 10.3389/fpsyg.2014.00353
    1. Nouri F, Lincoln N. An extended activities of daily living scale for stroke patients. Clinical Rehabilitation. 1987;1(4):301–5.
    1. Bickerton WL, Riddoch MJ, Samson D, Balani AB, Mistry B, Humphreys GW. Systematic assessment of apraxia and functional predictions from the Birmingham Cognitive Screen. J Neurol Neurosurg Psychiatry. 2012;83(5):513–21. doi: 10.1136/jnnp-2011-300968
    1. Hsieh YW, Hsueh IP, Chou YT, Sheu CF, Hsieh CL, Kwakkel G. Development and validation of a short form of the Fugl-Meyer motor scale in patients with stroke. Stroke. 2007;38(11):3052–4. doi: 10.1161/STROKEAHA.107.490730
    1. Zigmond AS, Snaith RP. The Hospital Anxiety and Depression Scale. Acta Psychiat Scand. 1983;67(6):361–70. doi: 10.1111/j.1600-0447.1983.tb09716.x
    1. Heitz RP. The speed-accuracy tradeoff: history, physiology, methodology, and behavior. Front Neurosci. 2014;8:150. doi: 10.3389/fnins.2014.00150
    1. Geusgens C, van Heugten C, Donkervoort M, van den Ende E, Jolles J, van den Heuvel W. Transfer of training effects in stroke patients with apraxia: an exploratory study. Neuropsychol Rehabil. 2006;16(2):213–29. doi: 10.1080/09602010500172350
    1. West C, Bowen A, Hesketh A, Vail A. Interventions for motor apraxia following stroke. Cochrane Database Syst Rev. 2008(1):CD004132. doi: 10.1002/14651858.CD004132.pub2
    1. Foley N, McClure JA, Meyer M, Salter K, Bureau Y, Teasell R. Inpatient rehabilitation following stroke: amount of therapy received and associations with functional recovery. Disabil Rehabil. 2012;34(25):2132–8. doi: 10.3109/09638288.2012.676145
    1. Dworzynski K, Ritchie G, Playford ED. Stroke rehabilitation: long-term rehabilitation after stroke. Clin Med (Lond). 2015;15(5):461–4. doi: 10.7861/clinmedicine.15-5-461
    1. Kwakkel G, Kollen B, Lindeman E. Understanding the pattern of functional recovery after stroke: facts and theories. Restor Neurol Neurosci. 2004;22(3–5):281–99.
    1. Sentinel Stroke National Audit Programme. National Results—Clinical. 2020 Accessed 24 September 2020.
    1. Lambercy O, Lehner R, Chua K, Wee SK, Rajeswaran DK, Kuah CWK, et al.. Neurorehabilitation From a Distance: Can Intelligent Technology Support Decentralized Access to Quality Therapy? Front Robot AI. 2021;8:612415. doi: 10.3389/frobt.2021.612415
    1. Berger VW. Selection bias and covariate imbalances in randomised clinical trials: John Wiley & Sons, Chichester; 2005.
    1. Fergusson D, Glass KC, Waring D, Shapiro S. Turning a blind eye: the success of blinding reported in a random sample of randomised, placebo controlled trials. BMJ. 2004;328(7437):432. doi: 10.1136/
    1. Schulz KF, Altman DG, Moher D, Fergusson D. CONSORT 2010 changes and testing blindness in RCTs. Lancet. 2010;375(9721):1144–6. doi: 10.1016/S0140-6736(10)60413-8

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