N/A N=296 Randomized Supportive Care

Electronic Social Network Assessment Program (eSNAP) + Caregiver Navigator

Brain Cancer

Bottom Line

View on ClinicalTrials.gov: NCT04268979 ↗

Enrolled (actual)

296

Serious AEs

—

Results posted

Oct 2025

Primary outcome: Primary: Family Caregiver Well-Being Using GAD-7 Scale — 8.95 score on a scale

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: eSNAP (Behavioral); Caregiver Navigator (Behavioral)
Age: Adult, Older Adult · 21+ yrs
Sex: All
Sponsor: H. Lee Moffitt Cancer Center and Research Institute
Primary completion: Jul 2024

Outcome Measures

Outcome	Result	p-value
PRIMARY Family Caregiver Well-Being Using GAD-7 Scale	8.95	—
PRIMARY Family Caregiver Well-Being Using PHQ-8 Scale	7.11	—
PRIMARY Family Caregiver Well-Being Using Zarit Burden Interview	13.77	—
PRIMARY Neuro Patients Well-Being Using GAD-7 Scale	5.66	—
PRIMARY Neuro Patients Well-Being Using PHQ-8 Scale	7.91	—
PRIMARY Neuro Patients Well-Being Using NeuroQol	40.9	—

Summary

The purpose of the study is to determine if family caregivers of neuro-oncology patients feel less burdened by utilizing the Electronic Social Network Assessment Program (eSNAP) + the Caregiver Navigator.

Eligibility Criteria

Inclusion Criteria

English-speaking/reading/writing
Able to complete questionnaires (including by proxy)
Family Caregivers (FCGs) must self-identify as being a primary FCG of a patient with a primary brain tumor, secondary (metastatic) brain tumor, or leptomeningeal disease diagnosis. A primary caregiver is a family member, friend, or other unpaid person who provides at least some care for a patient at home.
Patients must be diagnosed with new or recurrent primary brain tumor, a secondary (metastatic) brain tumor or leptomeningeal disease within the last 9 months, receiving at least some evaluation and/or care at Moffitt (i.e. at least one appointment), have a prognosis of at least 9 months

Exclusion Criteria

Patients may not participate without a consenting FCG, but FCGs may participate without a consenting patient
Patients and FCGs who are experiencing acute distress will be excluded from enrollment and referred directly to social work, per Moffitt policy.

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04268979). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.