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Glioblastoma Psychosocial Support Program

NCT06038604 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 11

Last updated 2024-07-31

No results posted yet for this study

Summary

The goal of the study is to conduct a pilot test of the psychosocial support intervention with family caregivers and/or patients coping with glioblastoma.

Conditions

Interventions

BEHAVIORAL

Psychosocial Support Intervention

Participants will receive six weekly 60-minute sessions conducted by videoconference.

Sponsors & Collaborators

Principal Investigators

  • Laura S. Porter, PhD · Duke University

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-11-03
Primary Completion
2024-06-25
Completion
2024-06-25

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06038604 on ClinicalTrials.gov