Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Anxiety
  • Caregiver Burden
  • Malignant Glioma
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: None (Open Label)Primary Purpose: Supportive Care

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

This study will be a prospective, randomized controlled trial to assess the efficacy of a caregiver-directed intervention designed to improve anxiety in caregivers of patients with malignant gliomas, in comparison with caregivers who receive usual care. The aim of this study is to test the efficacy ...

This study will be a prospective, randomized controlled trial to assess the efficacy of a caregiver-directed intervention designed to improve anxiety in caregivers of patients with malignant gliomas, in comparison with caregivers who receive usual care. The aim of this study is to test the efficacy of this intervention in reducing distress in caregivers of patients with malignant gliomas, in comparison with usual care. The study will be conducted in 120 caregivers.

Tracking Information

NCT #
NCT04109209
Collaborators
Conquer Cancer Foundation
Investigators
Principal Investigator: Deborah Forst, MD Massachusetts General Hospital