Multidomain Lifestyle Intervention in Mild Cognitive Impairment: Subgroup Analysis of the SUPERBRAIN-MEET Randomized Trial.

Da Ae Kim, Sun Min Lee, Kyunghwa Sun, Ji Hyun Park, Yoo Kyoung Park, Jee Hyang Jeong, Chang Hyung Hong, Jiwoo Jung, Hae Ri Na, Soo Hyun Cho, Hyun Sook Kim, Hong-Sun Song, Muncheong Choi, Bon D Ku, Yeonsil Moon, Hyun Jeong Han, Yun Jeong Hong, Eun-Joo Kim, Geon Ha Kim, Ko Woon Kim, Hyemin Jang, Soo Jin Yoon, Hee-Jin Kim, Seong Hye Choi, So Young Moon

Journal: Neurology 2026;107(3):e218297

PMID: 42475653

Abstract

BACKGROUND AND OBJECTIVES

Mild cognitive impairment (MCI) is a high-risk stage for progression to dementia. The SUPERBRAIN-MEET trial previously demonstrated cognitive benefits of a multidomain lifestyle intervention (MLI) delivered through face-to-face sessions and digital platforms. The aim of this study was to examine whether the cognitive effects of the MLI varied according to sociodemographic characteristics, digital readiness, baseline cognitive status, and vascular risk profiles, in a prespecified subgroup analysis of the SUPERBRAIN-MEET randomized controlled trial.

METHODS

SUPERBRAIN-MEET was a 24-week, multicenter, outcome assessor-blinded, parallel-group randomized controlled trial conducted across 17 hospitals in South Korea. Adults aged 60-85 years with MCI were randomly assigned (1:1) to the MLI or control group. Subgroups were defined based on sociodemographic factors (sex, age, education, and living status), digital readiness (internet access, frequency of digital device use), cognitive status (MMSE score), and vascular risk profiles (body mass index [BMI], obesity status, smoking status, systolic and diastolic blood pressure, serum total cholesterol, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, fasting plasma glucose, and cardiovascular comorbidity). The primary outcome was the change in the repeatable battery for the assessment of neuropsychological status (RBANS) total index score from baseline to 24 weeks. Effect modification was assessed using linear mixed-effects models with interaction terms and false discovery rate correction.

RESULTS

Of 300 randomized participants, 277 participants (mean age, 72.9 years; 69.3% female) were included in the modified intention-to-treat analysis (142 in the MLI group and 135 in the control group). MLI significantly improved RBANS total index scores compared with control at 24 weeks (between-group difference, 4.17 points; 95% CI 1.92-6.43). No subgroup interactions remained significant after false discovery rate correction, indicating consistent effects across subgroups.

DISCUSSION

In this subgroup analysis of the SUPERBRAIN-MEET trial, the cognitive benefits of MLI were not significantly modified by sociodemographic factors, digital readiness, baseline cognitive status, or vascular risk profiles. These findings should be interpreted with caution, given the exploratory nature of subgroup analyses and limited statistical power. The results support the generalizability and scalability of technology-assisted multidomain lifestyle interventions for dementia prevention in older adults with MCI.

TRIAL REGISTRATION INFORMATION

The trial was registered at ClinicalTrials.gov (NCT05023057; submitted August 20, 2021; first patient enrolled September 3, 2021; URL: clinicaltrials.gov/study/NCT05023057).

Address: Department of Neurology, Ajou University School of Medicine, Suwon, Republic of Korea.; National Institute of Dementia, National Medical Center, Seoul, Republic of Korea.; Department of Neurology, National Medical Center, Seoul, Republic of Korea.; Office of Biostatistics, Medical Research Collaborating Center, Ajou Research Institute for Innovative Medicine, Ajou University Medical Center, Suwon, Republic of Korea.; Department of Medical Nutrition, Graduate School of East-West Medical Nutrition, Kyung Hee University, Yongin, Republic of Korea.; Department of Neurology, Ewha Womans University College of Medicine, Seoul, Republic of Korea.; Department of Psychiatry, Ajou University School of Medicine, Suwon, Republic of Korea.; Rowan Inc., Seoul, Republic of Korea.; Department of Neurology, Bobath Memorial Hospital, Seongnam, Republic of Korea.; Department of Neurology, Chonnam National University Medical School, Gwangju, Republic of Korea.; Department of Neurology, CHA Bundang Medical Center, CHA University, Seongnam, Republic of Korea.; Department of Physical Education, Gyeongkuk National University, Andong, Republic of Korea.; Exercowork, Hanam, Republic of Korea.; Department of Neurology, Catholic Kwandong University International St. Mary's Hospital, Incheon, Republic of Korea.; Department of Neurology, Konkuk University Medical Center, Konkuk University School of Medicine, Seoul, Republic of Korea.; Ilsan Brain Neurology Clinic, Goyang, Republic of Korea.; Department of Neurology, Uijeongbu St. Mary's Hospital, The Catholic University of Korea, Uijeongbu, Republic of Korea.; Department of Neurology, Pusan National University Hospital, Pusan National University School of Medicine and Medical Research Institute, Busan, Republic of Korea.; Department of Neurology, Jeonbuk National University Medical School, Jeonju, Republic of Korea.; Department of Neurology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.; Department of Neurology, Eulji University Hospital, Eulji University School of Medicine, Daejeon, Republic of Korea.; Department of Neurology, Hanyang University College of Medicine, Seoul, Republic of Korea; and.; Department of Neurology, Inha University College of Medicine, Incheon, Republic of Korea.
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