Adaptive Digital Exercise Rehabilitation for Children After CHD Surgery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age6-12
SponsorThe Children's Hospital of Zhejiang University School of Medicine

About this trial

The goal of this clinical trial is to evaluate whether a Just-in-Time Adaptive Intervention (JITAI)-based digital exercise rehabilitation program can improve postoperative recovery in children after congenital heart disease (CHD) surgery. The study will examine whether this system can:

Improve cardiopulmonary endurance, cardiac function, and muscle strength Increase rehabilitation adherence and enhance training experience while reducing exercise-related fear Researchers will compare children receiving the adaptive digital exercise rehabilitation program with those receiving standard postoperative rehabilitation to determine whether the digital program provides additional clinical and behavioral benefits.

Participants will:

Wear non-invasive monitoring devices to collect real-time physiological data Engage in daily structured exercise rehabilitation sessions guided by the digital system Receive adaptive adjustments in exercise intensity based on real-time physiological feedback Complete questionnaires on recovery, emotional status, and rehabilitation experience

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Children aged 6 to 12 years

Diagnosed with congenital heart disease (CHD) and have undergone cardiac surgery

Clinically stable after transfer to the general ward, with stable circulatory, respiratory, musculoskeletal, and neurological status, and assessed by the clinician as suitable to begin active exercise rehabilitation

Able to understand and cooperate with basic exercise training requirements

Disqualifiers

Absolute contraindications to exercise rehabilitation, including uncontrolled arrhythmia, acute heart failure, hemodynamic instability, severe aortic stenosis, acute myocarditis, or acute pericarditis

Severe comorbid conditions that could interfere with rehabilitation, including severe hepatic or renal dysfunction, malignancy, or acute infection

Musculoskeletal or neuromuscular disorders that would prevent participation in or completion of the rehabilitation training

Trial design

Design model

Parallel

Treatments tested in this trial

  • JITAI-Based Digital Exercise Rehabilitation Program

    Behavioral

    This behavioral intervention uses a Just-in-Time Adaptive Intervention (JITAI)-based digital rehabilitation program to provide individualized exercise guidance for children recovering from congenital heart disease (CHD) surgery. The program integrates wearable monitoring devices with a digital rehabilitation platform to deliver real-time exercise prompts, adaptive training intensity adjustments, and continuous feedback based on physiological signals and exercise performance. During the intervention, participants receive structured postoperative exercise training that includes daily activity guidance, monitoring of heart rate and oxygen saturation, safety alerts, and automated recommendations to support adherence and optimize training effectiveness. The system aims to improve cardiopulmonary endurance, functional capacity, and recovery-related behaviors while ensuring safety through real-time monitoring and adaptive adjustments.

  • Standard Exercise Rehabilitation Program

    Behavioral

    A conventional post-operative exercise rehabilitation program based on existing pediatric cardiac rehabilitation guidelines. The program includes routine breathing training, early mobilization, and graded activity exercises supervised by clinical staff. No adaptive algorithm or real-time system-driven adjustments are used. Wearable devices may be used for data collection only, without influencing the intervention.

Treatment groups

130 Participants
are divided into 2 treatment groups
Group A: Adaptive Digital Rehabilitation (JITAI-Based) GroupExperimental treatment 1 intervention
Group B: Standard Rehabilitation Care GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Change in Six-Minute Walk Distance (6MWD)

Six-minute walk distance will be measured to assess changes in functional exercise capacity in children after congenital heart disease surgery. The outcome will compare the improvement in 6MWD between the adaptive digital rehabilitation group and the usual care group.

Time frame
Baseline to post-intervention (approximately 7-10 days postoperative period)
2

Cardiac Function Parameters (LVEF, FS)

Left ventricular ejection fraction (LVEF) assessed via echocardiography to evaluate changes in cardiac function following rehabilitation. Higher values indicate better cardiac performance. Measurements will be compared across study arms.

Time frame
Baseline to Post-intervention (within 7-10 days after surgery)
3

Lower Extremity Muscle Strength

Assessment of lower-limb muscle strength using standardized pediatric strength testing (e.g., manual muscle testing or dynamometer as applicable). Measures reflect postoperative physical recovery and response to the adaptive rehabilitation intervention.

Time frame
Baseline to Post-intervention (within 7-10 days after surgery)

Secondary outcomes

1

Training Adherence Rate

Percentage of prescribed training sessions completed by participants. Higher percentage indicates better adherence.

Time frame
Assessed at discharge
2

Change in Exercise Fear (TSK-C Score)

Change in fear of movement/exercise measured using the Tampa Scale for Kinesiophobia for Children (TSK-C). Total scores range from 11 to 44, with higher scores indicating worse kinesiophobia (greater fear of movement/exercise) and lower scores indicating improvement.

Time frame
From baseline to 4 weeks after the intervention
3

Exercise enjoyment score

Participant-reported exercise enjoyment measured using a child-appropriate version of the Physical Activity Enjoyment Scale (PACES). Total scores range from 16 to 80, with higher scores indicating greater enjoyment and a more positive exercise experience.

Time frame
Within 24 hours after completion of the intervention
4

Incidence, number, and type of exercise-training safety events

Incidence, number, and type of safety events occurring during exercise training, including abnormal heart rate, oxygen desaturation, unstable blood pressure, or early termination of treatment due to prespecified safety criteria.

Time frame
From baseline (first exercise training session) through hospital discharge, up to [30 days].

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

The Children's Hospital of Zhejiang University School of Medicine

Lead sponsor

Children's Hospital of Nanjing Medical University

Collaborator

Beijing Children's Hospital

Collaborator

This trial is not recruiting at the moment. You can still explore other options: