Multidisciplinary lifestyle interventions for neurological disorders during the Silent phase (MINDS) study: a multi-omics randomized controlled trial protocol

• Published in: Neurological research and practice 2024-08, Vol.6 (1), p.39-9, Article 39
• Main Authors: Taylor, Sara, Sachdeva, Seerat, Darling, Sandra, Arrotta, Kayela, Gallagher, Lisa, Supan, Alexis, Shipta, Gabrielle, Perko, Jim, Bar, Judi, James, Joe, Petschek, Iris, Lioi, Anthony, Kundu, Suman, Ellison, Lisa, Bekris, Lynn M, Willard, Belinda, Sangwan, Naseer, Mata, Ignacio, Fernandez, Hubert, Katzan, Irene, Conway, Devon, Pillai, Jagan, Leverenz, James, Busch, Robyn M, Floden, Darlene, Saper, Robert, Barnard, John, Machado, Andre, Najm, Imad, Punia, Vineet
• Format: Article
• Language: English
• Subjects: Alzheimer's disease; Biomarkers; Clinical Trial Protocol; Clinical trials; Cognition & reasoning; Cognitive ability; Diagnosis; Epilepsy; Intervention; Lifestyle interventions; Lifestyles; Music therapy; Neurodegenerative diseases; Neuroimaging; Neurological diseases; Neurological disorders; Older people; Parkinson's disease; Stroke
• ISSN: 2524-3489; 2524-3489
• DOI: 10.1186/s42466-024-00334-3

Given the prevalence and staggering cost of neurological disorders, there is dire need for effective early detection and intervention tools. Emerging evidence suggests that multidisciplinary lifestyle interventions (MLI) may mitigate the risk and progression of neurological disorders. The objectives of this protocol are (1) to test the impact of MLI on the progression of neurological disorders and (2) to identify multi-omic biomarkers for early stages of neurological disease and the impact of MLIs on these biomarkers. We present the Multidisciplinary lifestyle Interventions for Neurological Disorders during the Silent phase (MINDS) protocol, a randomized controlled trial of MLI in neurologically healthy older adults (≥ 50 years old) exhibiting elevated risk for common neurological disorders: stroke, epilepsy, Parkinson's Disease, or Alzheimer's disease and related dementias. Participants will be randomly assigned to intervention (n = 100) or control (n = 100) groups. The intervention group will receive 3 months of weekly 2-hour sessions on diet education, yoga, music therapy, and cognitive skills training. The participants' neurological health and engagement in relevant lifestyle practices will be assessed at regular intervals for 12 months. Neuroimaging and samples for multi-omic analyses will be collected at baseline, and at 3 months and 12 months after enrollment. Primary outcomes will be signs of progression of the neurological disorder risk that qualified them for study enrollment or a clinical diagnosis of the disorder. Secondary and exploratory outcomes will be based on self-reported health and multi-omic data. Data analysis will include between-group and longitudinal within-group analyses. The MINDS protocol and trial aims to clarify the impact of MLI on the progression of neurological disorder risk or diagnosis in older adults and to identify biomarkers that can be used to confirm MLI efficacy. The ability to validate the impact of MLI on neurological disorder progression based on biomarker data allows the identification of individuals most likely to benefit from such therapies in the early stages of neurological disease. The trial is registered on the National Institutes of Health (NIH) ClinicalTrials.gov (NCT05984056) site. It was registered on August 2nd, 2023. The trial has full approval of the Cleveland Clinic Internal Review Board.