The proposed study is a pilot study that aims to understand if the Pi Electronics adaptive music intervention (AM) is effective to promote positive psychosocial and cognitive outcomes, over and above a traditional music intervention (TM) among healthy older adults. This study will contribute to the ongoing literature on the benefits of music interventions and provide insight on how emerging technology can enhance the therapeutic effects of music as a viable intervention for older adults. The study will adopt a three-arm randomized controlled trial (RCT). Eligible participants will be randomized into one of three groups: traditional music therapy group (TM), Pi Electronic's adaptive music program (AM), and a waitlist control group (CG). Informed consent will be collected from all participants. All three groups will complete outcome measures at three sessions: pretest, posttest, and at a three-month follow-up, but only the TM and AM group will receive music between the pretest and posttest sessions, spanning for 4 weeks, with 4 music therapy sessions per week, and each session lasting 30 minutes. Data will be analyzed for each outcome variables to understand the group differences in the performance on the psychosocial and cognitive outcome measures. The study will also validate the Pi Electronics EEG headset with the BioSemi, 64-channel EEG system.
Age range
65 Years
Sex
ALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Quality of life: Psychosocial functions of healthy older adults.
Timeframe: Baseline (pretest), 4 weeks (posttest), and 16 weeks (3-month follow-up),
Resiliency: Psychosocial functions of healthy older adults.
Timeframe: Baseline (pretest), 4 weeks (posttest), and 16 weeks (3-month follow-up),
Emotional Regulation: Psychosocial functions of healthy older adults.
Timeframe: Baseline (pretest), 4 weeks (posttest), and 16 weeks (3-month follow-up),
Activities of Daily Living: Psychosocial functions of healthy older adults.
Timeframe: Baseline (pretest), 4 weeks (posttest), and 16 weeks (3-month follow-up),
Loneliness: Psychosocial functions of healthy older adults.
Timeframe: Baseline (pretest), 4 weeks (posttest), and 16 weeks (3-month follow-up),
Emotional processing: Cognitive functions of healthy older adults.
Timeframe: Baseline (pretest), 4 weeks (posttest), and 16 weeks (3-month follow-up),
Processing Speed: Cognitive functions of healthy older adults.
Timeframe: Baseline (pretest), 4 weeks (posttest), and 16 weeks (3-month follow-up),