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i Anna P Wolf University of Tasmania A Thesis Submitted in Partial Fulfillment of the Requirements PDF

412 Pages·2016·2.96 MB·English
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Preview i Anna P Wolf University of Tasmania A Thesis Submitted in Partial Fulfillment of the Requirements

IDENTIFICATION AND PREDICTION OF INTER-INDIVIDUAL DIFFERENCES IN COGNITIVE TRAINING TRAJECTORIES: A GROWTH MIXTURE MODELLING APPROACH Anna P Wolf University of Tasmania A Thesis Submitted in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy (Clinical Psychology) in the School of Psychology. June 2015 All rights reserved. This thesis may not be reproduced in whole or in part, by photocopy or other means, without the permission of the author. i ii ABSTRACT There is emerging evidence of inter-individual differences in cognitive training responsiveness. Conventional statistics do not adequately address heterogeneity and longitudinal performance trajectories. Generalised growth mixture modelling (GGMM; Muthén, 2004) was utilised to identify and predict heterogeneous longitudinal cognitive performance trajectories following training. Specific and generalised effects of training were examined. Baseline characteristics such as age, sex and proxies for cognitive reserve were also explored as predictors of trajectories. Data from 315 community-dwelling older adults (age 55–85 years) from the Active Cognitive Enhancement (ACE) Program training study were analysed. Short-term (VM) and long-term verbal memory (LTVM) and executive functioning (EF) were tested using the Rey Auditory Verbal Learning Test (RAVLT) and the CogState Ltd Groton Maze Learning Test (GMLT) at baseline and at 3-, 6- and 12-month follow- ups. Generalised growth mixture modelling demonstrated High, Moderate, and Low performance classes for memory performance. High and Low classes were identified for executive function. Also identified were demonstrable performance trajectory gains in the trained individuals of the Low class for executive function, those performing at a low normative level at baseline (Cohen’s d = 2.23). These results offer a novel contribution to the literature. Gains by those trained in the Low performing VM and LTVM classes’ performance trajectories were also shown (Cohen’s d = 4.48 and 1.38, respectively). However, the iii experimental participants were compared to a small number of controls (n = 2) thus no meaningful training effects on memory were identified. The GGMM models therefore demonstrated that the multidomain ACE cognitive training program produced some generalised cognitive improvement in healthy older adults, albeit to limited extent. Age and estimated premorbid IQ (a proxy for cognitive reserve) predicted Low EF performance trajectories compared to High class performances. Trained individuals were more likely to be older and have lower levels of estimated pre-morbid IQ. Individuals who demonstrated executive function performance gains were less likely to demonstrate verbal memory trajectory gains. These findings suggest distinct responses to training in different cognitive domains and/or distinctive inter-individual responses to elements of the multi-domain training program. Caution with interpretation of GGMM labels and predictive factors identified is necessary, given their relativity to the cohort. With this approach, current theories including compensation, magnification, ‘Use It or Lose It’, plasticity, flexibility, and cognitive reserve are supported. Application of GGMM can also further facilitate development of individually tailored and cost effective cognitive training programs. iv DECLARATION This thesis contains no material which has been accepted for a degree or diploma by the University or any other institution, and to the best of the my knowledge and belief no material previously published or written by another person except where due acknowledgement is made in the text of the thesis, nor does the thesis contain any material that infringes copyright. Signed: Date: 12/1/2016 STATEMENT OF AUTHORITY OF ACCESS This thesis may be made available for loan and limited copying in accordance with the Copyright Act of 1968. Signed: Date: 12/1/2016 v vi ACKNOWLEDGEMENTS Firstly, I’d like to thank the Australian Research Council (ARC), in collaboration with Alzheimer’s Australia, Tasmania (AATas), Department of Health and Human Services (DHHS), and the School of Psychology, University of Tasmania (UTas) for their generous funding support to implement this ambitious research project. To my primary supervisor, Jeff, thank you for taking me on as one of your students and your encouragement to do a PhD. Thank you for sharing with me some of your immense academic wisdom. I am so grateful for your instrumental assistance in seeing me through the inevitable (multiple) hurdles along the way. Thank you also for your fantastic anecdotes about university life, research and your travels, which always made supervision such a pleasure. To my co-supervisor Rapson, thank you for your enthusiasm when coming on board the research team, and for introducing me to, and assisting me with implementing growth mixture modelling. Without this assistance, this PhD could not have come about. To my second co-supervisor Mathew, thank you for your assistance with the study’s development, and your clinical expertise and guidance during the running of the program. I’m also very appreciative of your thorough and useful feedback about the final document. To Sarah, thank you for not only being instrumental in the development and implementation of the ACE project as a whole, but for your professional support and your caring friendship. vii To Malcolm, for being such a committed ACE developer, facilitator and instigator of those much needed coffee meetings! To Avril, thank you for your tireless research assistant work and your generous hospitality in Tasmania. To Amy, for your fantastic editing assistance. In particular thank you for being so thorough and generous with your time and effort. To all those who participated in the research study, as well as all the volunteers who devoted their time to the ACE project – thank you all for your integral contributions, enthusiasm and commitment. To my treasured friends and family both near and far. I love you all dearly. You kept me going! I can’t wait to have loads more spare time now to continue the fun! To Anastasia, thank you for your friendship, thoughtfulness and crazy ways. You do make me laugh! To Leonie, thanks for all the fun times, “walkie talkies”, and of course for our continuing friendship for all these years. To Dani - Wifey! Thank you for sharing the “nanna rug” time, and for being such a honest and caring friend. To Sinead, thank you for our fantastic long chats at Uni, Alzheimer’s, cafes and via Skype! I look forward to more! To Vandita, for your friendship in both Tassie and Sydney. Just hearing your voice instantaneously fills my heart with joy! viii To Eddy, for welcoming me so openly to Hobart, for your assistance with surviving the “smelly boys” and for continuing to share your life with me. To Dave, Buddy, thank you for always being such a loving brother! I miss you now you’re in Canada, but I’m so happy you’re so happy over there. I know you’ll always be there for me. To DiDi, thank you for your open ear and being such a nurturing aunty. To Alan, thanks for our stimulating chats about movies, politics and for sharing your amazing cooking and incredible travel photos! Joan for being such a kind, caring and immensely compassionate person. I am so grateful for all your unyielding support and understanding. I’m also so thankful for you sharing your home with me and for our family dinners! Finally to my extraordinary parents, Penny and John. Words cannot fully encapsulate how much gratitude I have for your undying love, support, dear friendship and mentorship all the way through this long journey. Mum, Dad, what can I say? I simply couldn’t have done it without you. ix x

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other rehabilitation studies (Chu et al., 2007; Fairchild et al., 2013). Chu and colleagues (2007) also used a multi-level modelling approach to measure recovery in new learning and memory following traumatic brain injury. They found that factors such as age only predicted the level of cognitive ou
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