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NCT Number: NCT04237519

The StayFitLonger Study: an Innovative Computerized Home-based Training to Foster Independent Life at Home

Multimodal training, including physical and cognitive activities, has been associated with a reduction in age-related physical and cognitive decline. Therefore, combining these activities into a home-based computerized training program may represent a powerful approach to foster independent life at home. The StayFitLonger study is a 6-month multi-site randomized controlled, double-blind trial, which tests the efficacy of a home-based computerized intervention that combines physical and cognitive exercises through virtual coaching to enhance motivation.

In Switzerland, Canada and Belgium, a total of 128 older participants will be recruited and randomly assigned to one of two physical and cognitive home-based interventions for 6 months: StayFitLonger or active control training. The StayFitLonger intervention provides physical and cognitive training exercises, feedback and instructions through a virtual coach to optimize motivation. It also offers social and psycho-educational contents. Monthly supervision (home-visits and phone calls) will be provided during this 6-month intervention. Outcomes will be measured at baseline, and after 6 months of training.

This study will demonstrate the feasibility, sustainability and efficacy of a home-based multi-domain intervention program allowing further development and possible commercialization of a scientifically validated training program to slow down cognitive and physical decline.

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Key information

Age range

60 year–100 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

BRUSANO (ASBL - Association Sans But Lucratif), Brussels, Belgium

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About this study

Finding ways to improve and maintain functional abilities and quality of life in older people has become a worldwide priority. It is well recognized that reduced engagement in physical, cognitive and social activities has negative influence on the health of older adults. This leads to more vulnerabilities both physically and cognitively. Sedentary behaviors can ultimately induce physical frailty, defined as a state of high vulnerability with accumulation of adverse health outcomes. Fear of falling and/or unsteady gait are common factors of physical frailty. Moreover, falls are particularly common in older adults. In addition to mobility limitation and falls, cognitive decline has been identified as a major cause of disability and dependency in older populations.

Through non-pharmacological interventions focusing on alterable lifestyle factors, experts believe in the possibility to protect older people from the deleterious effects of physical and brain aging that can lead to dementia. In other words, keeping a healthy mind in a healthy body might be the gold standard for healthy aging. Several studies have shown that physical activity, through aerobic, gait and strength training, induces many beneficial effects including improvement of general health, cognition and quality of life. In addition, a growing number of cognitive interventions have been conducted in healthy seniors and older adults with mild cognitive impairment (MCI) and results show improved cognition and delayed cognitive decline. As well, cognitive deficits, mainly in executive functions, have been associated with an increase number of falls and abnormal gait among others.

Improvement of these physical functions was observed in response to cognitive interventions. Because aging is complex and different interventions are likely to potentiate their effects, an increasing number of studies have reported on combined interventions targeting two or more modifiable factors. However, accessibility to these interventions remain a major challenge because older adults may not have access to specialized expertise and resources.

The use of a computerized system to deliver lifestyle interventions have several advantages: it can be used to support home-based training, reducing costs and increasing access; training can be self-paced and last over practically a unlimited time; it allows providing immediate feedback; it offers potential for scaling up for wider use if efficacy is proven; it provides an excellent interface for active control interventions. Surprisingly, whereas many studies assessed computerized cognitive training programs, only a few have used home-based interventions which combine cognitive training with physical activity and, to our knowledge, only one study used computerized tasks for both physical and cognitive training in healthy older adults.

The StayFitLonger study was designed to test efficacy of a home-based computerized training program targeted at older adults, which combine physical exercises and cognitive training. The main goal of the program is to improve physical health and prevent frailty through an innovative approach using videos of 50 physical exercises focusing on gait and strength, which could be easily implemented in older adults (Test-and-Exercise home-based program). The program was also designed to enhance cognitive functions through a series of activities in form of serious games. These activities train executive control through dual-task exercises that was found to increase divided attention and frontal lobe function general knowledge learning and problem solving training. Other features of the program that are unique include: 1) Prospective memory exercises embedded in the physical exercises; 2) Social interactions whereby participants can create and share with other participants their learning material and can chat with their peers about topics of interest and find solutions to common real-life problems; 3) Psycho-educational content on cognition, physical health, nutrition and on ways to apply newly learned strategies in real life to empower participants and promoting self-management; 4) A virtual coach aimed to improve adherence by guiding participants, reminding them to use the program regularly, and providing feedback and rewards through a system of virtual credits; 5) Possibility to personalize the application settings to tailor the environment to the participant's tastes and wishes; 6) Wearable motion sensors used during physical exercises for movement detection as a game input and for providing measurements on mobility for a better characterization of the potential benefits of the program.

The StayFitLonger study will test the effect of the training on key outcomes using a double-blind, parallel-group, randomised control trial (RCT) over 6 months. The primary objective is to assess whether the 6-month StayFitLonger programme leads to better performance than those observed following the active control condition on the Timed-Up & Go (TUG), a functional physical task, which is associated with lower-body strength and balance. The efficacy study also includes a few secondary objectives. One is to assess whether the StayFitLonger programme improves other physical capabilities as well as cognitive performances and scores of affective variables (e.g., mood, fear of falling), and psycho-social domains (e.g., quality of life, daily living activities, participant's expectation). In addition, the study will also assess whether a similar gain is found in robust vs pre-frail seniors.

In Switzerland, Canada and Belgium, a total of 128 older participants will be recruited. Following the initial eligibility screening, participants will be randomized to one of two home-based computerized intervention conditions, the StayFitLonger training program (experimental) or the active control training program . Enrolled participants will be evaluated at two time points: at baseline (T0) and after 6 months of training (T1, end of the RCT). The training will take place at home for 6 months. Prior to the start of the training and within a month following T0 assessment, introductory courses in groups of a maximum of 6 people will take place to introduce the features of the program and describe the different physical and cognitive exercises. Participants will be supervised through home visits and monthly phone calls to ensure a good use of the program in both groups.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Fluent french speaker adults
  • Retired, living at home and having a wireless Internet connection in their house;
  • Independent for all daily activities (optimal score to the 4-IADL);
  • Open to the use of new technologies and electronic tablets;
  • Interested in exercising to stay fit;
  • Able to walk without a walking aid (e.g. wheelchair, sticks, walker, etc.);
  • Available to commit themselves for the time period during which the study takes place;
  • No vision deficits that would prevent them to read information on a tablet;
  • No current neurological or psychiatric diagnosis (e.g. Parkinson's disease).

Exclusion criteria

  • MoCA score < 26;
  • score ≥ 3 on the Fried's frailty index (Fried et al., 2001)

Treatment and study plan

SFL training

Behavioral

The SFL training program comprises:

  • Physical exercises: 50 video exercises to improve balance, muscle strength and physical capabilities in older adults;
  • Cognitive exercises: Four ludic activities targeting problem solving (4 Images/ 1 word), memory (Quiz and Recall me), speed processing and divided attention (Attention!).

In addition, the SFL program includes a series of unique components:

  • Chat rooms: to share views about topics of interest and tips for common real-life problems;
  • Psycho-education content: to improve self-management and promoting cognitive transfer though 22 different topics (provide recommendations usually given in psychotherapy sessions);
  • Virtual coach: to guide participants along the proposed exercises by giving them instructions, reminding them regularly to practice a variety of available activities repeatedly, providing appropriate and timely feedback on participant's performances and rewarding assiduity, perseverance and performance.

Active controlled training

Behavioral

The active control training program is structured in the same manner as the SFL training program and will also offer different physical and cognitive activities:

  • Physical exercises: 12 different exercises trains upper and lower extremity strength, mobility and balance offered through a computerized version of a health insurance company physical training program;
  • Cognitive activities: Four commercially available leisure activities (Sudoku. Cross Words, Pac-Man and Countdown activities) that are appreciated by older adults but do not teach cognitive strategies and are were not designed to improve cognition per se.

No chat room, psycho-educational content or virtual coach were included in the active control training program.

Primary outcomes

  1. Timed-Up & Go Test (TUG)

    Time frame: T0 (baseline)

    To measure lower extremity function, mobility and risk of falls

  2. Timed-Up & Go Test (TUG)

    Time frame: T1 (six months following T0)

    To measure lower extremity function, mobility and risk of falls

Secondary outcomes

  1. Physical domain: Twenty-meter walking test

    Time frame: T0 (baseline)

    To measure gait speed in sec.

  2. Physical domain: Twenty-meter walking test

    Time frame: T1 (six months following T0)

    To measure gait speed in sec.

  3. Physical domain: Five Time Sit to Stand Test (FTSTS)

    Time frame: T0 (baseline)

    To measure lower extremity strength in sec

  4. Physical domain: Five Time Sit to Stand Test (FTSTS)

    Time frame: T1 (six months following T0)

    To measure lower extremity strength in sec

  5. Physical domain: Four Stage Balance Test (FSBT)

    Time frame: T0 (baseline)

    To measure balance. A total score of 4 is obtained when a participant performs successfully 4 positions (parallel, semi-tandem and tandem). The test is stopped when a participant fails at holding a given position for at least 10 sec.

  6. Physical domain: Four Stage Balance Test (FSBT)

    Time frame: T1 (six months following T0)

    To measure balance. A total score of 4 is obtained when a participant performs successfully 4 positions (parallel, semi-tandem and tandem). The test is stopped when a participant fails at holding a given position for at least 10 sec.

  7. Physical domain: motion sensors measures

    Time frame: T0 (baseline)

    During TUG and 20-m walking test, motion sensors will provide measures on: walking speed, variability in gait, stance phase, foot-flat phase, double support, stride velocity, maximal swing speed, turning angle and variability in toe clearance.

  8. Physical domain: motion sensors measures

    Time frame: T1 (six months following T0)

    During TUG and 20-m walking test, motion sensors will provide measures on: walking speed, variability in gait, stance phase, foot-flat phase, double support, stride velocity, maximal swing speed, turning angle and variability in toe clearance.

  9. Cognitive domain: Global cognition composite score

    Time frame: T0 (baseline)

    This score is the ZAVEN composite score computed by averaging z-scores from:

    • Total recall of the California Verbal Learning Test (CVLT) and delayed recall of the WMS-IV Logical Memory to measure episodic memory;
    • WAIS-IV Digit Symbol substitution Test (DSST) to measure complex attention;
    • Verbal fluency (VF) to measure executive functions.
  10. Cognitive domain: Global cognition composite score

    Time frame: T1 (six months following T0)

    This score is the ZAVEN composite score computed by averaging z-scores from:

    • Total recall of the California Verbal Learning Test (CVLT) and delayed recall of the WMS-IV Logical Memory to measure episodic memory;
    • WAIS-IV Digit Symbol substitution Test (DSST) to measure complex attention;
    • Verbal fluency (VF) to measure executive functions.
  11. Cognitive domain: Memory composite score

    Time frame: T0 (baseline)

    This score is computed by averaging z-scores from:

    • Delayed recall of the CVLT;
    • Delayed recall of the WMS-IV Logical Memory Test.
  12. Cognitive domain: Memory composite score

    Time frame: T1 (six months following T0)

    This score is computed by averaging z-scores from:

    • Delayed recall of the CVLT;
    • Delayed recall of the WMS-IV Logical Memory Test.
  13. Cognitive domain: Executive composite score

    Time frame: T0 (baseline)

    This score is computed by averaging z-scores from:

    • Verbal fluency (VF);
    • Trail Making Test (condition B - A; shifting - processing speed scores);
    • Victoria Stroop (high interference - naming conditions);
    • Divided attention subtest from the Test of Attention Performance 2.3.1 (number of total omissions (visual and auditory)).
  14. Cognitive domain: Executive composite score

    Time frame: T1 (six months following T0)

    This score is computed by averaging z-scores from:

    • Verbal fluency (VF);
    • Trail Making Test (condition B - A; shifting - processing speed scores);
    • Victoria Stroop (high interference - naming conditions);
    • Divided attention subtest from the Test of Attention Performance 2.3.1 (number of total omissions (visual and auditory)).
  15. Cognitive domain: Speed processing composite score

    Time frame: T0 (baseline)

    This score is computed by averaging z-scores from:

    • Trail Making Test (time on condition A);
    • DSST (number of correct symbols);
    • Victoria Stroop (time on naming condition).
  16. Cognitive domain: Speed processing composite score

    Time frame: T1 (six months following T0)

    This score is computed by averaging z-scores from:

    • Trail Making Test (time on condition A);
    • DSST (number of correct symbols);
    • Victoria Stroop (time on naming condition).
  17. Affective domain: Hospital Anxiety and Depression Scale (HADS)

    Time frame: T0 (baseline)

    To measure mood.

  18. Affective domain: Hospital Anxiety and Depression Scale (HADS)

    Time frame: T1 (six months following T0)

    To measure mood.

  19. Affective domain: Falls Efficacy Scale International (FES-I)

    Time frame: T0 (baseline)

    To measure fear of falling.

  20. Affective domain: Falls Efficacy Scale International (FES-I)

    Time frame: T1 (six months following T0)

    To measure fear of falling.

  21. Psycho-social domain: Older People Quality of Life questionnaire (OPQOL 35).

    Time frame: T0 (baseline)

    To measure quality of Life (QoL)

  22. Psycho-social domain: Older People Quality of Life questionnaire (OPQOL 35).

    Time frame: T1 (six months following T0)

    To measure quality of Life (QoL)

  23. Psycho-social domain: Cognitive Function Instrument (CFI) -

    Time frame: T0 (baseline)

    To measure subjective difficulties encountered in activities of daily living, related to cognitive functions

  24. Psycho-social domain: Cognitive Function Instrument (CFI) -

    Time frame: T1 (six months following T0)

    To measure subjective difficulties encountered in activities of daily living, related to cognitive functions

  25. Psycho-social domain: Everyday Cognition (E-Cog)

    Time frame: T0 (baseline)

    To measure subjective difficulties encountered in activities of daily living, related to cognitive functions

  26. Psycho-social domain: Everyday Cognition (E-Cog)

    Time frame: T1 (six months following T0)

    To measure subjective difficulties encountered in activities of daily living, related to cognitive functions

  27. Psycho-social domain: Ad-hoc questionnaire

    Time frame: T0 (baseline)

    To measure participant's expectation from the training program. The questionnaire is related to the efficacy of the program and its different components, the expectation (difficulty, agreeableness, motivation) and the quality of the introductory courses.

  28. Psycho-social domain: Ad-hoc questionnaire

    Time frame: T1 (six months following T0)

    To measure participant's expectation from the training program. The questionnaire is related to the efficacy of the program and its different components, the expectation (difficulty, agreeableness, motivation) and the quality of the introductory courses.

  29. Cognitive processes manipulated during training: ad-hoc computerized test

    Time frame: T0 (baseline)

    To measure divided attention trained during Attention! activity with an ad-hoc computerized test designed specifically for this multitasking activity and provided in the form of a serious game.

  30. Cognitive processes manipulated during training: ad-hoc computerized test

    Time frame: T1 (six months following T0)

    To measure divided attention trained during Attention! activity with an ad-hoc computerized test designed specifically for this multitasking activity and provided in the form of a serious game.

  31. Cognitive processes manipulated during training: Rivermead Behavioural Memory Test - Third edition (RBMT-3).

    Time frame: T0 (baseline)

    To measure prospective memory trained in the Quiz activity with two subtests ("belonging" and "appointment")

  32. Cognitive processes manipulated during training: Rivermead Behavioural Memory Test - Third edition (RBMT-3).

    Time frame: T1 (six months following T0)

    To measure prospective memory trained in the Quiz activity with two subtests ("belonging" and "appointment")

  33. Cognitive processes manipulated during training: Flexibility subtest from the Test battery for Attention Performance

    Time frame: T0 (baseline)

    To measure concept elaboration trained in the 4images/1 word activity with a "set shifting" computerized task

  34. Cognitive processes manipulated during training: Flexibility subtest from the Test battery for Attention Performance

    Time frame: T1 (six months following T0)

    To measure concept elaboration trained in the 4images/1 word activity with a "set shifting" computerized task

  35. Cognitive processes manipulated during training: Similitudes subtest from the WAIS-IV:

    Time frame: T0 (baseline)

    To measure concept elaboration trained in the 4images/1 word activity and assess verbal reasoning and the development of concepts.

  36. Cognitive processes manipulated during training: Similitudes subtest from the WAIS-IV:

    Time frame: T1 (six months following T0)

    To measure concept elaboration trained in the 4images/1 word activity and assess verbal reasoning and the development of concepts.

Other outcomes

  1. Effects of moderators on primary and secondary outcomes: Age

    Time frame: Age measured within a month prior to the start of the intervention

    To see the influence of age on primary and secondary outcomes using 2 age groups defined by the median

  2. Effects of moderators on primary and secondary outcomes: Sex

    Time frame: Sex measured within a month prior to the start of the intervention

    To see the influence of sex on primary and secondary outcomes using 2 sex groups (male and female)

  3. Effects of moderators on primary and secondary outcomes: Education

    Time frame: Education measured within a month prior to the start of the intervention

    To see the influence of education on primary and secondary outcomes using 2 education groups (less or more than 12 years)

Sponsors and collaborators

Lead sponsor

University of Lausanne Hospitals

Other

Collaborators

  • Active and Assisted Living Programme
  • BRUSANO
  • Centre de Recherche de l'Institut Universitaire de Geriatrie de Montreal
  • HES-SO Valais-Wallis
  • Haute-Ecole Arc
  • Mindmaze SA
  • Pro-Senectute Vaud
  • Université Catholique de Louvain

Registry information

Official study title

StayFitLonger. Preventive Effects of a Combination of Non-drug Interventions (Physical, Cognitive and Social) in Healthy Elderly Subjects: Multicentre Randomised Controlled Trial.

Acronym: SFL

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Jan 23, 2020
Registry last updated
Aug 18, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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