Impact of Nutrition, Sleep, and Physical Activity on Intellectual Function and Muscle Mass in Older Adults (INSPIOR)

Impact of Notifications on Nutrition, Sleep, and Physical Activity on Intellectual Function and Muscle Mass in OldeR Adults (INSPIOR)

The goal of this prospective, single site, interventional randomized control trial is to treat age related health conditions in adults older than 65 years and functional independence. The main question of the study is to answer the effectiveness of notification on activity, sleep, and nutrition based on wearable device Fitbit recorded data for the improvement of health conditions including intellectual property and physical function, compared to usual care. Participants in the intervention arm will be given a Fitbit Charge 5 device and asked to wear this for the duration of the study, including during sleep. The study intervention will run for 6 months. Notifications will be issued using a monitoring software in Japanese, and issued automatically to participants. Participants in the control arm will be given a routine care and health-related information. Researchers will compare cognitive performance, muscle mass and physical activity between the two groups to see if the notification based on Fitbit data would promote the health conditions of older adults.

Study Overview

• Status: Completed
• Conditions: Cognitive Function; MCI; Cognition Disorders in Old Age; Frailty/Sarcopenia
• Intervention / Treatment: Device: Fitbit wearing, with notification for sleep, activity and nutrition based fitbit data; Device: Routine care

Detailed Description

This is a prospective, single site, interventional randomized control trial. The primary purpose is to treat age related health conditions. The current study is nested within an established cohort based in Kashiwa City in Japan, which consists of older adults living independently. The inclusion criteria of this study is age equal to or older than 65 years and functional independence (i.e., not requiring nursing care provided by long-term care insurance). The investigators plan to conduct a randomized controlled trial to test the effectiveness of notification based on Fitbit recorded data, used to prompt health and wellness actions on a variety of health outcomes, compared to usual care. On enrollment, baseline demographic and health information as well as baseline measurements for quality of life, and physical and mental health, will be collected. Subsequently, the study intervention will run for 6 months. Participants in the intervention arm will be given a Fitbit Charge 5 device and asked to wear this for the duration of the study, including during sleep. Participants will receive sessions to teach them how to use the Charge 5 device and access the information produced. Those who meet the above criteria for intervention will receive automatically generated notifications that include lifestyle recommendations. Notifications will be issued using a monitoring software in Japanese, and issued automatically as text alerts to participants. Participants will receive encouraging notifications to promote adherence and health condition. Participants in the control arm will be given a routine care and health-related information. Participants who fail to exhibit a behavior change in the week following the alert, or who are not engaging with the study (e.g., by not wearing the Fitbit device) will be followed up by phone by a member of the community research group. Researchers will compare cognitive performance and physical activity between the two groups to see if the notification based on Fitbit data would promote the health conditions of older adults. Results of this trial will be valuable for informing further implementation of wearable devices and related digital devices in elderly populations in Japan and other countries in the region.

• Study Type: Interventional
• Enrollment (Actual): 355
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Japan
  • Chiba
    • Kashiwa, Chiba, Japan, 2778562
      • Graduate School of Frontier Sciences, The University of Tokyo

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Older Adult
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

• Over 65 years of age.
• Living in Japan.
• Living independently with or without carer support.
• Able and willing to wear a Fitbit for the duration of the study (≥20 hours a day, including during sleep).
• Individuals that are able and willing to receive and act on interventions.
• Has capacity to consent to inclusion in the study.
• Smartphone access to allow Fitbit installation and setup.

• Has one or more of the following comorbidities:

  • BMI <20 (65-69 years), <21.5 (≥70 years)
  • Pre-frail or Frail: scoring 1-2 (pre-frail) or 3+ (frail) based on the FRAIL questionnaire
  • Sarcopenia: low grip strength (female <18 kg, male <28 kg); Gait speed (< 1m/s); low Skeletal Muscle mass Index (female 5.7 kg/m2; male 7 kg/m2)

Exclusion Criteria:

• Individuals receiving full time care in a care facility.
• Individuals that are unable to receive and/or act on interventions.
• Individuals who are existing wearable users, or who have prior experience using a wearable to manage their health.
• Individuals with uncontrolled hypertension, diabetes, CKD or with cardiac pacemakers and/or cardiovascular stent(s).
• Individuals who have any additional condition or situation that the Investigator (PI) or designee determines as inappropriate for participation in this study.
• Individuals with no comorbidities as defined above.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Prevention
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: Intervention; Notification on Nutrition, Sleep, and Physical Activity based on fitbit-based data	Device: Fitbit wearing, with notification for sleep, activity and nutrition based fitbit data; Notification on Nutrition, Sleep, and Physical Activity based on fitbit-based data, and Nutritional supplementation and Promotion of Exercise
Sham Comparator: Control; Regular Care	Device: Routine care; Regular Care on sleep, activity and nutrition

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Executive function	TMT	0 - 6 months
General Cognition	MoCA	0 - 6 months
Muscle mass	Skeletal Muscle mass Index	0 - 6 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Amount of exercise	Step counts measured by fitbit	0 - 6 months
Amount of sleep	Total sleep time measured by fitbit	0 - 6 months

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
Frail/Sarcopenia	Frailty index	0 - 6 months
Malnutrition	Protein intake	0 - 6 months

Collaborators and Investigators

• Sponsor: Tokyo University
• Collaborators: Google LLC.
• Investigators: Principal Investigator: Tatsuhiro Hisatsune, PhD, Associate professor

Study record dates

Study Major Dates

• Study Start (Actual): November 8, 2023
• Primary Completion (Actual): July 31, 2024
• Study Completion (Actual): July 31, 2025

Study Registration Dates

• First Submitted: November 13, 2023
• First Submitted That Met QC Criteria: November 13, 2023
• First Posted (Actual): November 18, 2023

Study Record Updates

• Last Update Posted (Actual): April 16, 2026
• Last Update Submitted That Met QC Criteria: April 13, 2026
• Last Verified: April 1, 2026

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Neurologic Manifestations; Nervous System Diseases; Neuromuscular Manifestations; Pathologic Processes; Pathological Conditions, Anatomical; Muscular Atrophy; Atrophy; Pathological Conditions, Signs and Symptoms; Signs and Symptoms; Frailty; Sarcopenia
• Other Study ID Numbers: 22-360

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No