AI-driven Personalized Exercise Feedback Program on Exercise Adherence in Traumatic Brain Injury

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorNational Defense Medical Center, Taiwan

About this trial

This study aims to develop and evaluate an AI-driven Personalized Exercise Feedback Program (AI-PEF) to enhance exercise adherence and health outcomes in mTBI patients.

Methods: AI-PEF integrates the transtheoretical model and self-determination theory with machine learning algorithms to provide real-time, personalized feedback. A phased randomized controlled trial will be conducted: Phase I evaluates feasibility and acceptability through Delphi methods with expert consensus and patient feedback; Phase II validates preliminary outcomes with 30 participants in a 2-arm randomized trial; and Phase III assesses the program's impact on adherence, sleep quality, depressive symptoms, and quality of life with 90 participants in a 3-arm randomized trial.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Eligible participants are patients aged over 18 with mild TBI (GCS 13-15)

who can walk independently,

reside in the Greater Taipei area,

and possess sufficient Chinese or Taiwanese language proficiency to understand the trial

Disqualifiers

Exclusion criteria include individuals with severe medical conditions (e.g., respiratory failure, epilepsy, psychiatric disorders), musculoskeletal or neurological impairments

hindering physical activity in the 6-minute walk test,

cognitive impairments (MMSE < 24),

frontal lobe injuries or penetrating injury causing significant psychological dysfunction.

Trial design

Design model

Parallel

Treatments tested in this trial

  • AI-PEF

    Behavioral

    Participants will follow a 12-week walking program with five 30-minute sessions per week, progressively increasing intensity based on heart rate and effort indices. Garmin fitness trackers will monitor adherence and intensity. Remote guidance will support participants via weekly digital health messages on the LINE app, offering personalized feedback, goal reinforcement, and lifestyle recommendations. Participants will also receiThese AI feedback implementations will be tailored to complement the in-person education and will include reminders of the individualized goals set during the remote exercise intervention and consultation . The digital component will also offer a platform for patients to share their progress and seek further guidance during the scheduled in-person consultation. The use of digital AI feedback aligns with the trend of integrating technology into healthcare services, providing a convenient and accessible modality for supporting parents engaging in regular exercise.

  • Theory-based digital exercise

    Behavioral

    The theory-based digital exercise group will follow the same in-person clinic visits and walking program as AI-PEF but without AI-driven feedback

  • Active Control

    Behavioral

    Participants in the active control group will receive standard TBI care, including Garmin-based self-monitoring and routine clinic visits at baseline (T0), 3 months (T1), and 6 months (T2). These visits will include general health education and recommendations on daily physical activity. No personalized or digital exercise strategies will be provided. Participants completing the 6-month protocol will have the option to access the AI-PEF program after the study.

Treatment groups

125 Participants
are divided into 3 treatment groups
Group A: AI-PEFExperimental treatment 1 intervention
Group B: Theory-based digital exerciseExperimental treatment 1 intervention
Group C: Active control groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Adherence

Exercise adherence will be the primary outcome, defined as the percentage of participants completing at least five exercise sessions weekly over 12 weeks. Adherence will be objectively tracked using the Garmin Vivosmart 5, which monitors exercise duration and frequency. Range of adherence are 0- 100%, the higher percentage means the higher adherence.

Time frame
T1-baseline
2

Adherence

Exercise adherence will be the primary outcome, defined as the percentage of participants completing at least five exercise sessions weekly over 12 weeks. Adherence will be objectively tracked using the Garmin Vivosmart 5, which monitors exercise duration and frequency. Range of adherence are 0- 100%, the higher percentage means the higher adherence.

Time frame
T2- 1 month later
3

Adherence

Exercise adherence will be the primary outcome, defined as the percentage of participants completing at least five exercise sessions weekly over 12 weeks. Adherence will be objectively tracked using the Garmin Vivosmart 5, which monitors exercise duration and frequency. Range of adherence are 0- 100%, the higher percentage means the higher adherence.

Time frame
T3- 2 month later
4

Adherence

Exercise adherence will be the primary outcome, defined as the percentage of participants completing at least five exercise sessions weekly over 12 weeks. Adherence will be objectively tracked using the Garmin Vivosmart 5, which monitors exercise duration and frequency. Range of adherence are 0- 100%, the higher percentage means the higher adherence.

Time frame
T4- 3 month later

Secondary outcomes

1

The Revised Sport Motivation Scale-II

The Revised Sport Motivation Scale-II (SMS-II), validated in Chinese, will measure six types of motivation, including amotivation, external regulation, introjected regulation, identified regulation, integrated regulation, and intrinsic motivation. A total of 18 items with Likert scale 1-7, 5 domains: Intrinsic Regulation: 3, 9, 17, Integrated Regulation: 4, 11, 14, Identified Regulation: 6, 12, 18, Introjected Regulation: 1, 7, 16, External Regulation: 5, 8, 15, Non Regulation: 2, 10, 13. Each domain is record separately. The higher scores means the higher tendency of the domain. The range of the minimum and maximum values are 18-126.

Time frame
T1- baseline
2

The Revised Sport Motivation Scale-II

The Revised Sport Motivation Scale-II (SMS-II), validated in Chinese, will measure six types of motivation, including amotivation, external regulation, introjected regulation, identified regulation, integrated regulation, and intrinsic motivation. A total of 18 items with Likert scale 1-7, 5 domains: Intrinsic Regulation: 3, 9, 17, Integrated Regulation: 4, 11, 14, Identified Regulation: 6, 12, 18, Introjected Regulation: 1, 7, 16, External Regulation: 5, 8, 15, Non Regulation: 2, 10, 13. Each domain is record separately. The higher scores means the higher tendency of the domain. The range of the minimum and maximum values are 18-126.

Time frame
T2- 1 month later
3

The Rivermead Post-Concussion Symptoms Questionnaire

The Rivermead Post-Concussion Symptoms Questionnaire (RPQ) will assess physical, cognitive, and behavioral symptoms associated with TBI, validated for mild to moderate TBI cases. A total of 16 items, scored 0-4, ranged 0- 64, the higher scores mean the severity of the concussion symptoms.

Time frame
T1 baseline
4

The Beck Depression Inventory-II

The Beck Depression Inventory-II (BDI-II), with total scores categorized as follows: 0-13 (normal), 14-19 (mild depression), 20-28 (moderate depression), and 29-63 (severe depression), will evaluate depressive symptoms with established reliability (α = 0.94) and validity.

Time frame
T1 baseline

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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