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AI-Personalized Digital Exercise for University Students

Effects of an AI-Personalized Digital Exercise Programme on Adherence, Physical Activity, and Wellbeing Among University Students: An 8-Week Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07825948
Acronym
AIPDEUS
Enrollment
299
Registered
2026-09-17
Start date
2026-01-24
Completion date
2026-03-21
Last updated
2026-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Exercise Adherence, Physical Activity, Wellbeing

Keywords

Artificial Intelligence, Digital Health, University Students, Exercise Adherence, Physical Activity, Personalized Exercise, Exercise Program, Wellbeing, Randomized Controlled Trial, Mobile Health

Brief summary

This study evaluated whether an AI-personalized digital exercise programme could improve exercise adherence, physical activity, wellbeing, and physical performance among university students compared with a standardized digital exercise programme. University students were randomly assigned to one of two digital exercise programmes for 8 weeks. The AI-personalized programme adjusted exercise recommendations using participant characteristics, previous exercise adherence, readiness, pain, safety information, and physical performance measures. The comparator provided a standardized digital exercise programme without adaptive weekly personalization. The primary outcome was mean weekly exercise adherence. Secondary outcomes included physical activity, wellbeing, countermovement jump performance, lower-limb reaction time, engagement, usability, and safety.

Detailed description

This was an 8-week, two-group randomized controlled trial conducted among undergraduate students at Transilvania University of Brașov, Romania. The study compared an AI-personalized digital exercise programme with a standardized digital exercise programme delivered within the same digital study environment. Participants assigned to the AI-personalized group received exercise recommendations through MoveAI-Student version 2.1.0 using the version-controlled v1.3-adaptive system. The system combined prespecified safety rules with a supervised recommendation model. Personalization used participant characteristics, sport participation, weekly training volume, countermovement jump performance, simple and choice reaction time, readiness, pain, previous-week adherence, and safety information. Exercise recommendations could specify session frequency, duration, intensity, and additional emphasis on lower-limb power or reactive drills. Recommendations were updated once per intervention week. Progression was limited by predefined safety rules, and exercise load could be reduced when pain or an adverse-event flag was present. Human override of recommendations was permitted when required. Participants assigned to the standardized digital comparator used the same digital study environment but did not receive the adaptive weekly prescription procedure. The comparator programme prescribed three exercise sessions per week, with each session lasting 35 minutes. The primary outcome was mean weekly exercise adherence, calculated from completed sessions relative to prescribed sessions across the 8-week intervention. Secondary outcomes included total physical activity assessed with the International Physical Activity Questionnaire Short Form, WHO-5 wellbeing, countermovement jump performance, simple reaction time, choice reaction time, moderate-to-vigorous physical activity, application engagement, satisfaction, perceived usefulness, usability, sitting time, body weight, body mass index, and adverse events. The study was designed to estimate the effect of the adaptive programme as a complete intervention compared with standardized digital exercise. It was not designed to isolate the independent effect of the algorithm from differences in exercise prescription or completed exercise exposure.

Interventions

BEHAVIORALAI-Personalized Digital Exercise Programme

An 8-week digital exercise intervention using MoveAI-Student version 2.1.0 and the v1.3-adaptive system. Initial exercise prescriptions ranged from three to five sessions per week, 30 to 45 minutes per session, at moderate-to-vigorous intensity. Recommendations were updated weekly using adherence and safety information. Prescriptions could modify session frequency, duration, intensity, and emphasis on lower-limb power or reactive drills. Predefined safety rules limited weekly progression and allowed reduced exercise load when pain or an adverse-event flag was present.

BEHAVIORALStandardized Digital Exercise Programme

An 8-week standardized digital exercise intervention delivered through the same study application. Participants were prescribed three exercise sessions per week, with each session lasting 35 minutes. The programme did not use the adaptive weekly prescription procedure applied in the AI-personalized group.

Sponsors

Transilvania University of Brasov
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

Participants were randomized after completion of baseline assessments to one of two parallel groups for 8 weeks: an AI-personalized digital exercise programme or a standardized digital exercise programme.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

Undergraduate student currently enrolled at Transilvania University of Brașov. Age 18 to 65 years at baseline. Written informed consent provided before any study-specific procedure. Able to safely complete the standardized countermovement jump protocol using OptoJump. Able to safely complete the lower-limb simple and choice reaction-time protocols using BlazePod. Access to a smartphone compatible with the study application. Willing to use the study application throughout the 8-week intervention. Able to attend both baseline and post-intervention assessments.

Exclusion criteria

Acute musculoskeletal injury or pain that made jumping or rapid lower-limb responses unsafe. Medical condition contraindicating exercise participation or study testing. Use of medication known to affect neuromuscular performance or reaction time, as defined in the approved protocol. Concurrent participation in another interventional exercise or digital-health trial. Inability or unwillingness to complete the required assessments or the 8-week digital intervention.

Design outcomes

Primary

MeasureTime frameDescription
Mean Weekly Exercise AdherenceFrom intervention initiation through the end of Week 8Weekly adherence was calculated as completed exercise sessions relative to prescribed exercise sessions within each intervention week. The participant-level mean across the 8-week intervention was used as the primary outcome.

Secondary

MeasureTime frameDescription
Total Physical ActivityBaseline and at the end of Week 8Total physical activity was assessed using the International Physical Activity Questionnaire Short Form (IPAQ-SF) and expressed as MET-minutes per week.
WHO-5 Well-Being ScoreBaseline and at the end of Week 8Wellbeing was assessed using the WHO-5 Well-Being Index.
Countermovement Jump Best HeightBaseline and at the end of Week 8Best countermovement jump height was assessed using OptoJump Next and expressed in centimeters.
Countermovement Jump Mean HeightBaseline and at the end of Week 8Mean countermovement jump height was assessed using OptoJump Next and expressed in centimeters.
Simple Reaction TimeBaseline and at the end of Week 8Description: Lower-limb simple reaction time was assessed using BlazePod and expressed in milliseconds.
Choice Reaction TimeBaseline and at the end of Week 8Lower-limb choice reaction time was assessed using BlazePod and expressed in milliseconds.

Countries

Romania

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 18, 2026