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Testing a Palliative and Supportive Care Program for Children with Cancer to Improve Their Comfort and Quality of Life

Embedded Model of Integrated Paediatric Palliative Care in Paediatric Oncology: Development and Testing its Effectiveness. (EMANCIPATION Study) - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/090800
Enrollment
300
Registered
2025-07-14
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Health Condition 1: C00-D49- Neoplasms

Interventions

Intervention1: Paediatric specific palliative care model: A structured pediatric palliative care model embedded into oncology workflows delivered by a palliative nurse and psychologist in coordination

Sponsors

Indian Council of Medical Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Intervention Group 1 Children aged 2 to 18 years with cancer 2 Receiving care at participating hospitals 3 Eligible for palliative care as per treating team 4 Primary caregiver willing to consent and participate 5 Able to complete assessments at baseline 4 and 8 weeks Comparator Group 1 Children aged 2-18 years with cancer 2 Receiving routine oncology care without palliative care 3 Caregiver willing to participate and complete follow up

Exclusion criteria

Exclusion criteria: Intervention Group 1. Severe cognitive or developmental issues 2. Expected survival less then 4 weeks 3. Language barriers preventing tool use 4. Caregiver unwilling to consent or follow-up. 1. Already receiving structured palliative care 2. Cognitive limitations 3. Language or logistical barriers 4. Caregiver not consenting or non-adherent to follow-up

Design outcomes

Primary

MeasureTime frame
Feasibility and preliminary impact of a structured pediatric palliative care intervention on symptom burden and health-related quality of life in children with cancerTimepoint: Outcomes will be assessed at three time points baseline preintervention 4 weeks mid intervention and 8 weeks post intervention.

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Naveen Salins

Kasturba Medical College, Manipal University

naveensalins@gmail.com08202922221

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026