Physical ACtivity and Exercise Outcomes in Huntington Disease (PACE-HD): Protocol for a 12-Month Trial Within Cohort Evaluation of a Physical Activity Intervention in People With Huntington Disease.

BACKGROUND Exercise is emerging as an important aspect in the management of disease-related symptoms and functional decline in people with Huntington disease (HD). Long-term evaluation of physical activity and exercise participation in HD has yet to be undertaken. OBJECTIVE The objective is to investigate the feasibility of a nested randomized controlled trial (RCT) alongside a longitudinal observational study of physical activity and exercise outcomes in people with HD. DESIGN This will be a 12-month longitudinal observational study (n = 120) with a nested evaluation of a physical activity intervention (n = 30) compared to usual activity (n = 30) using a "Trial within a Cohort" (TWiC) design. SETTING The study will take place in HD specialist clinics in Germany, Spain, and the USA, with intervention delivery in community settings. PARTICIPANTS The participants will be those with early-mid stage HD participating in the 'Enroll-HD' study. INTERVENTION This will be a 12-month physical activity behavioral change intervention, delivered by physical therapists in 18 sessions, targeting uptake of aerobic exercise and increased physical activity. MEASUREMENTS All participants (n = 120) will complete Enroll-HD assessments (motor, cognitive, behavioral, and quality of life) at baseline and 12 months. Additional Physical ACtivity and Exercise Outcomes in Huntington Disease (PACE-HD) assessments include fitness (predicted VO2 max), self-reported and quantitative measures of physical activity, disease-specific symptoms, and walking endurance. RCT participants (n = 60) will complete an additional battery of quantitative motor assessments and a 6-month interim assessment. Enroll-HD data will be linked to PACE-HD physical activity and fitness data. LIMITATIONS The limitations include that the embedded RCT is open, and assessors at RCT sites are not blinded to participant allocation. CONCLUSION PACE-HD will enable determination of the feasibility of long-term physical activity interventions in people with HD. The novel TWiC design and incorporation of data linkage has potential to reduce participant burden. This design could be applied to other neurological diseases and movement disorders where recruitment and retention are challenging.

[1]  L. Quinn,et al.  Client and therapist views on exercise programmes for early-mid stage Parkinson's disease and Huntington's disease , 2010, Disability and rehabilitation.

[2]  J. Wyatt,et al.  Better reporting of interventions: template for intervention description and replication (TIDieR) checklist and guide , 2014, BMJ : British Medical Journal.

[3]  K. R. Ridderinkhof,et al.  No Evidence That Frontal Eye Field tDCS Affects Latency or Accuracy of Prosaccades , 2018, bioRxiv.

[4]  L. Quinn,et al.  The societal cost of Huntington's disease: are we underestimating the burden? , 2016, European journal of neurology.

[5]  K. Lorig,et al.  Development and evaluation of a scale to measure perceived self-efficacy in people with arthritis. , 1989, Arthritis and rheumatism.

[6]  L. Quinn,et al.  Development and Delivery of a Physical Activity Intervention for People With Huntington Disease: Facilitating Translation to Clinical Practice , 2016, Journal of neurologic physical therapy : JNPT.

[7]  R. Ryan,et al.  Exercise, physical activity, and self-determination theory: A systematic review , 2012, International Journal of Behavioral Nutrition and Physical Activity.

[8]  L. Quinn,et al.  A randomized, controlled trial of a multi-modal exercise intervention in Huntington's disease. , 2016, Parkinsonism & related disorders.

[9]  Anne-Catherine Bachoud-Lévi,et al.  F63 Preliminary results from Q-MOTOR/Q-COG analyses in the repair-hd study , 2018 .

[10]  L. Quinn,et al.  Physical Therapy and Exercise Interventions in Huntington’s Disease: A Mixed Methods Systematic Review , 2017, Journal of Huntington's disease.

[11]  D. Rennie,et al.  SPIRIT 2013 statement: defining standard protocol items for clinical trials. , 2013, Annals of internal medicine.

[12]  D. Tulsky,et al.  HD-PRO-TRIAD™ Validation: A Patient-reported Instrument for the Symptom Triad of Huntington's Disease , 2014, Tremor and other hyperkinetic movements.

[13]  L. Quinn,et al.  Task-Specific Training in Huntington Disease: A Randomized Controlled Feasibility Trial , 2014, Physical Therapy.

[14]  A. Hannan,et al.  Environmental factors as modulators of neurodegeneration: Insights from gene–environment interactions in Huntington's disease , 2015, Neuroscience & Biobehavioral Reviews.

[15]  A. Rosser,et al.  Rethinking Functional Outcome Measures: The Development of a Novel Upper Limb Token Transfer Test to Assess Basal Ganglia Dysfunction , 2018, Front. Neurosci..

[16]  K. Malterud,et al.  Caregiver roles in families affected by Huntington's disease: a qualitative interview study. , 2014, Scandinavian journal of caring sciences.

[17]  R. Reilmann,et al.  A randomized, placebo‐controlled trial of AFQ056 for the treatment of chorea in Huntington's disease , 2015, Movement disorders : official journal of the Movement Disorder Society.

[18]  R. Reilmann,et al.  Motor outcome measures in Huntington disease clinical trials. , 2017, Handbook of clinical neurology.

[19]  G. Landwehrmeyer A Prospective Registry Study in a Global Huntington's Disease Cohort A CHDI Foundation Project , 2011 .

[20]  L. Quinn,et al.  Reliability and Minimal Detectable Change of Physical Performance Measures in Individuals With Pre-manifest and Manifest Huntington Disease , 2013, Physical Therapy.

[21]  Michael Catt,et al.  Validation of the GENEA Accelerometer. , 2011, Medicine and science in sports and exercise.

[22]  L. Quinn,et al.  Physical Activity Self-Management and Coaching Compared to Social Interaction in Huntington Disease: Results From the ENGAGE-HD Randomized, Controlled Pilot Feasibility Trial , 2017, Physical therapy.

[23]  L. Quinn,et al.  Exercise testing and training in people with Huntington’s disease , 2015, Clinical rehabilitation.

[24]  L. Quinn,et al.  A Randomized Feasibility Study of a 12-Week Community-Based Exercise Program for People With Huntington's Disease , 2013, Journal of neurologic physical therapy : JNPT.

[25]  Merit Cudkowicz,et al.  Motor, cognitive, and functional declines contribute to a single progressive factor in early HD , 2017, Neurology.

[26]  L. Quinn,et al.  What effect does a structured home-based exercise programme have on people with Huntington’s disease? A randomized, controlled pilot study , 2013, Clinical rehabilitation.

[27]  Francis O. Walker Huntington's Disease. , 2007 .

[28]  A. Carrón,et al.  Development and initial validation of the Brunel lifestyle physical activity questionnaire , 2005, British Journal of Sports Medicine.

[29]  A. Kaptein,et al.  Impact of Huntington's disease on quality of life , 2001, Movement disorders : official journal of the Movement Disorder Society.

[30]  B. Ainsworth,et al.  International physical activity questionnaire: 12-country reliability and validity. , 2003, Medicine and science in sports and exercise.

[31]  S. McEwen,et al.  Exercise-enhanced neuroplasticity targeting motor and cognitive circuitry in Parkinson's disease , 2013, The Lancet Neurology.

[32]  S. Kostyk,et al.  Video game play (Dance Dance Revolution) as a potential exercise therapy in Huntington’s disease: a controlled clinical trial , 2013, Clinical rehabilitation.

[33]  Jon Nicholl,et al.  Rethinking pragmatic randomised controlled trials: introducing the “cohort multiple randomised controlled trial” design , 2010, BMJ : British Medical Journal.

[34]  L. Quinn,et al.  Supporting physical activity engagement in people with Huntington’s disease (ENGAGE-HD): study protocol for a randomized controlled feasibility trial , 2014, Trials.

[35]  W. Kröger,et al.  Recommendations , 1915, Nature.