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Assessing Palliative Care Needs and Quality of Life in Children with Cancer

Screening for Palliative Care needs and exploring its association with Quality of Life in Children with Cancer - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/10/074943
Enrollment
108
Registered
2024-10-08
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

Health Condition 1: C64- Malignant neoplasm of kidney, except renal pelvis Health Condition 2: C40-C41- Malignant neoplasms of bone and articular cartilage Health Condition 3: C81-C96- Malignant neoplasms of lymphoid, hematopoietic and related tissue

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

Dr Vani Verma
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: For Children 1. Children are diagnosed with cancer, aged 2-18 years. 2. At least one month after the cancer diagnosis. 3. Able to communicate and read in either the local language, Kannada or English. For Caregivers: 1. Primary caregivers include father and/or mother, and if parents are not available, grandparents who provide care to children with cancer for a period exceeding one month. 2. Unpaid family caregivers of children with cancer. 3. Aged 18 years or older. 4. Able to communicate and read in either the local language, Kannada or English.

Exclusion criteria

Exclusion criteria: For Children: 1. Children with severe cognitive impairments affecting their ability to participate in the study 2. Being unwilling to give informed consent For Caregivers: 1. Severe cognitive impairments affecting their ability to participate in the study 2. Not being able to communicate verbally or orally 3. Being unwilling to give informed consent.

Design outcomes

Primary

MeasureTime frame
To explore the association of Palliative Care needs with Quality of Life in Children with Cancer.Timepoint: 24-30 months

Secondary

MeasureTime frame
a. To assess the Quality of Life in children with Cancer using PedsQLTM Cancer Module 3.0. b. To assess the Palliative Care needs in Children with Cancer using PaPaS scale. c. To measure the Caregiver Burden using “The Caregiving Burden Scale for Family Caregivers of Children with Cancers (CBSFC-CC) ? in a pediatric oncology settingTimepoint: 18-24 months to assess the Quality of Life in children with Cancer using PedsQLTM Cancer Module 3.0 and to assess the Palliative Care needs in Children with Cancer using PaPaS scale. 24-30 months to measure the Caregiver Burden using “The Caregiving Burden Scale for Family Caregivers of Children with Cancers (CBSFC-CC) ? in a pediatric oncology setting

Countries

India

Contacts

Public ContactDr Vasudeva Bhat K

Kasturba Medical College, Manipal

vasudev.bhat@manipal.edu9619114703

Outcome results

None listed

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