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Development of Family Intervention Program for parents of children with brian tumors

The Family intervention program for the parents of children with brain tumors: A Feasibility Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/109638
Enrollment
32
Registered
2026-04-28
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

None listed

Interventions

Intervention1: Family Intervention Program Group: The family intervention program will be developed using need assessment. Based upon the needs, a family intervention program will be developed and tes

Sponsors

University Grant Commission
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Parents of children diagnosed with Malignant brain tumors by the treating neurosurgery consultant of NIMHANS Hospital. Those parents of pediatric brain tumors willing to provide informed consent and actively participate in the family intervention program. Residing with the children for at least past 6 months. Those Parents who stay with the child during the phase of Hospitalization Aged between 21 to 50 years. Those who speak Kannada or English would be included.

Exclusion criteria

Exclusion criteria: Parents of Children with Traumatic Brain Injury Parents of children with other neurological and neurosurgical disorders Parents with the History of Mental illness. Parents with terminal illness. Parents with Pediatric Brain Tumors undergoing Gama Knife surgery. Parents who have previously participated in any other structured psychosocial intervention program.

Design outcomes

Primary

MeasureTime frame
The Primary outcomes of the intervention is to assess the feasibility of the Family intervention program through Acceptability of the program, Recruitment rates and Adherence and satisfaction. Along with this, the variable used here is Parental distress is the primary variable.Timepoint: for Parental distress, baseline assement, endline assessment and 1 month follow up assessment will be done.

Secondary

MeasureTime frame
The researcher would explore by analyzing within the group changes between 3 time points pre -post-follow upTimepoint: Baseline assessment, endline assessment & 1 month follow up assessment will be conducted

Countries

India

Contacts

Public ContactYatheesh Bharadwaj

National Institute of Mental Health And Neurosciences

ponnupsw@gmail.com7358466735

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026