The Effect of Therapeutic Play on Preoperative Anxiety in Hospitalized Children With Congenital Heart Disease

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age0-12
SponsorFirst Affiliated Hospital of Kunming Medical University

About this trial

Congenital Heart Disease (CHD) is the most common congenital malformation in children and the leading cause of death from birth defects in infancy. Preoperative anxiety is prevalent in children with CHD, but current preoperative care mainly focuses on physical preparation, with insufficient attention to psychological stress, and conventional intervention measures have limitations. As a non-pharmacological method, therapeutic play has been proven effective in relieving children's anxiety, but randomized controlled trials (RCTs) of therapeutic play for preoperative anxiety in children with CHD are still lacking in China. This study adopts a randomized controlled design, in which children with CHD before surgery are randomly divided into the experimental group and the control group. The experimental group receives therapeutic play (including parents' participation, with intervention content designed according to children's cognitive characteristics), while the control group receives routine preoperative nursing. The effect of therapeutic play on relieving preoperative anxiety in children with CHD will be evaluated multi-dimensionally through anxiety scale scores, vital signs, and salivary cortisol levels, providing scientific evidence for clinical intervention of preoperative anxiety in children with CHD.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Aged 0 to 12 years old, with basic communication and comprehension abilities to respond to play interventions and complete anxiety scale assessments.

Clear consciousness, no severe intellectual, hearing, or speech communication disorders, or pervasive developmental disorders (e.g., autism), and being able to interact with researchers.

Primary caregivers (father or mother) provide written informed consent and have the ability to understand the study and assist the child with the intervention.

Disqualifiers

Children with complex critical CHD requiring emergency surgery or admission to the intensive care unit (ICU) upon hospitalization.

Children with severe neurological disorders (e.g., cerebral palsy, epilepsy), severe hepatic/renal insufficiency, or other major congenital diseases that may affect psychological status or perioperative progress.

Children who have taken sedatives, anxiolytics, or antidepressants long-term preoperatively, whose anxiety levels have been altered by medication.

Participants who cannot complete the intervention or outcome assessments for any reason (e.g., surgery cancellation, withdrawal of consent).

Trial design

Design model

Parallel

Treatments tested in this trial

  • Therapeutic Play Intervention

    Behavioral

    Intervention Description :children receive routine preoperative preparation plus a structured, age-appropriate therapeutic play intervention. The play activities, involving parent-child interaction, are tailored to the child's cognitive level to distract attention, reduce fear, and relieve preoperative anxiety before congenital heart disease surgery.

  • Routine Preoperative Nursing

    Behavioral

    Standard preoperative care including fasting guidance, medication preparation, and health education.

Treatment groups

204 Participants
are divided into 2 treatment groups
Group A: Therapeutic Play GroupExperimental treatment 2 interventions
Group B: Routine Preoperative Care GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Anxiety levels of children

For children: Chinese Version of the Modified Yale Preoperative Anxiety Scale (m-YPAS), full scale range 23 \~ 100 points. Higher scores indicate greater preoperative anxiety (worse outcome); lower scores represent milder anxiety.

Time frame
Baseline (T0, pre-intervention), immediately post-intervention (T1), and during anesthesia induction (T2)
2

Anxiety levels of primary caregivers

For primary caregivers: State-Trait Anxiety Inventory (STAI, State Anxiety Subscale), full scale range 20 \~ 80 points. Higher scores indicate higher caregiver anxiety (worse outcome); lower scores mean less anxiety.

Time frame
Baseline (T0, pre-intervention), immediately post-intervention (T1), and during anesthesia induction (T2)

Secondary outcomes

1

Preoperative hospital satisfaction

Satisfaction with preoperative care will be assessed via self-developed satisfaction questionnaire completed by primary caregivers, with scores ranging from 0 to 100; higher scores correspond to better preoperative care satisfaction.

Time frame
At discharge from the preoperative ward (assessed up to 5 days)

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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