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Customized Neuro-Imaging Referenced Symptom Video for the Reduction of Patient and Caregiver Anxiety Around Radiation Treatment for Brain Tumors

M.D. Anderson Cancer Center · with National Cancer Institute (NCI) · NCT04479696

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18+ · All sexes
Healthy volunteers
Accepted
Study type
Interventional · Not applicable
Target enrollment
117
US sites recruiting
1
Study start
June 5, 2019
Record last updated
July 20, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

This trial studies whether a customized video intervention can help to reduce anxiety in brain cancer patients undergoing radiation treatment and their caregivers. A customized neuro-imaging referenced symptom video that describes symptoms and side effects specific to the patients' tumor may result in an early and sustained reduction in anxiety and distress during and after radiation treatment, thereby improving quality of life.

Being studied: Educational Intervention; Questionnaire Administration; Survey Administration; Video

Conditions: Glioblastoma; WHO Grade II Glioma; WHO Grade III Glioma

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • PATIENT ELIGIBILITY CRITERIA: Adult patients with newly diagnosed glioma (World Health Organization [WHO] grade 2-4) who are planned for a 6-week course of radiotherapy after surgery
  • PATIENT ELIGIBILITY CRITERIA: Able to complete questionnaires in English
  • PATIENT ELIGIBILITY CRITERIA: Has a post-operative diagnostic magnetic resonance imaging (MRI) of the brain with and without contrast acquired within 4 weeks of the start of radiotherapy
  • CAREGIVER ELIGIBILITY CRITERIA: Adult caregiver (>= 18 years) who is accompanying an eligible patient consented to the study
  • CAREGIVER ELIGIBILITY CRITERIA: The patient who the caregiver is accompanying is consented for participation on the study
  • CAREGIVER ELIGIBILITY CRITERIA: Able and willing to complete questionnaires in English

Exclusion Criteria

  • PATIENT ELIGIBILITY CRITERIA: Significant cognitive or psychiatric symptoms that prevent the ability to complete the questionnaires as determined by the assessing staff in the pre-intervention evaluation
  • PATIENT ELIGIBILITY CRITERIA: Poor performance status (Karnofsky performance status [KPS] \< 60) that prevent the ability to complete the questionnaires
  • CAREGIVER ELIGIBILITY CRITERIA: Significant cognitive or psychiatric symptoms that prevent the ability to complete the questionnaires as determined by the assessing staff in the pre-intervention evaluation

Recruiting US locations

  • M D Anderson Cancer Center

    Houston, TX 77030

    Site contact: Caroline Chung · 713-563-2300

Study contacts (from the official record)

  • Caroline Chung · 713-745-5422 · cchung3@mdanderson.org
Customized Neuro-Imaging Referenced Symptom Video for the… (NCT04479696) | Bored Studies