Parental Distress and Treatment Adherence in Pediatric Recurrent Medulloblastoma

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age0-18
SponsorWest China Hospital

About this trial

Children with medulloblastoma, an aggressive brain tumor, require prolonged and complex multimodal therapy. Their primary parental caregivers bear the main responsibility for ensuring treatment adherence, yet the psychological toll on these caregivers may undermine their ability to follow prescribed regimens. This study investigates whether multidimensional parental distress predicts overall treatment adherence in this population, and which specific distress domains are most strongly associated with poor adherence.

Parental distress-including depression, anxiety, and posttraumatic stress-is common among parents of children with cancer and may interfere with their ability to manage complex treatment regimens. However, no study has specifically examined whether parental distress predicts treatment adherence in children with recurrent medulloblastoma, a devastating brain tumor with a poor prognosis and no standard treatment protocol.

This prospective longitudinal cohort study aims to investigate whether parental distress is a significant predictor of treatment adherence in children with recurrent medulloblastoma. A total of 450 parent-child dyads will be enrolled across 4 tertiary pediatric oncology centers. Children must have a confirmed diagnosis of recurrent medulloblastoma and be receiving active treatment. Parents (primary caregivers) will complete validated questionnaires at baseline assessing depression, anxiety, stress, and trauma-related distress using the DASS-21 and IES-R. Treatment adherence will be monitored over a 12-month follow-up period using electronic medication monitoring caps, clinic attendance records, and parent-reported medication logs.

The primary outcome is the proportion of prescribed chemotherapy doses taken (treatment adherence rate). Secondary outcomes include trajectories of adherence over time and the relationship between specific dimensions of parental distress (depression, anxiety, stress, posttraumatic stress) and adherence patterns. The study will also examine whether child clinical factors (e.g., molecular subgroup, prior treatment history) and family demographic factors moderate this relationship.

Findings from this study may inform the development of targeted psychosocial interventions to support distressed parents and improve treatment adherence-and ultimately clinical outcomes-in this vulnerable pediatric population. Participants can expect to be enrolled in the study for approximately 12 months.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosis of medulloblastoma with documented recurrence (radiographic or histopathological confirmation)

Age ≤ 18 years at enrollment

Currently receiving active treatment for recurrent disease

Life expectancy ≥ 3 months

Disqualifiers

Child receiving exclusively palliative/hospice care

Parent with severe psychiatric illness or cognitive impairment preventing informed consent or questionnaire completion

Child enrolled in another interventional trial that would confound adherence measurement

Trial population

Parent-child dyads where child has recurrent medulloblastoma and is receiving active treatment

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Not applicable- observational study

    Other intervention

    Not applicable- observational study

Treatment groups

450 Participants
are divided into 1 treatment group
Group A: Parent-Child Dyads with Recurrent Medulloblastoma1 intervention

Trial outcomes

Primary outcomes

1

Overall Treatment Adherence Score

Composite adherence score (range 0-10) based on the 8-item Morisky Medication Adherence Scale (MMAS-8) plus clinic attendance and home-care behavior index. Higher scores indicate better adherence.

Time frame
12 months from enrollment

Secondary outcomes

1

Parenting Stress Index-Short Form (PSI-SF) Total Score

36-item scale assessing parental distress across three subdomains: Parental Distress, Parent-Child Dysfunctional Interaction, and Difficult Child. Range 36-180, higher scores indicate greater stress.

Time frame
12 months from enrollment
2

DASS-21 Subscale Scores

Depression, Anxiety and Stress Scale-21 scores for each subscale (range 0-21), with higher scores indicating greater symptom severity.

Time frame
12 months from enrollment

Other outcomes

Sponsors and contacts

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

West China Hospital

Lead sponsor

First Affiliated Hospital Xi'an Jiaotong University

Collaborator

Shanghai Children's Medical Center

Collaborator

Children's Hospital of Chongqing Medical University

Collaborator