Couples tackle brain tumors together with online Mind-Body program
NCT ID NCT03244995
First seen Jun 27, 2026 · Last updated Aug 13, 2026 · Updated 2 times
Summary
This study tests an online mind-body program designed for people with brain tumors (glioma) and their partners. The program aims to improve spiritual well-being, sleep, mood, and overall quality of life for both. Researchers are enrolling 74 couples to see if the program is practical and helpful.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Mind-Body Intervention (online couple-based program)
- What this could lead to
- If it works, this could offer a practical way to improve emotional and physical well-being for brain tumor patients and their partners.
- What could go wrong
- This is a small, early feasibility study (74 participants) focused on whether the program is acceptable, not on proving it works. Results may not apply to all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
74 people
The number who actually took part.
- Started
-
Aug 2017
- Expected to finish
-
Dec 2028
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * PATIENT ONLY: Patients with a diagnosis of HGG or low grade glioma (LGG), based on radiographic or pathologic diagnosis of grade III or IV listed in the medical records, or patients with a malignancy that has metastasized to the brain * PATIENT ONLY: Patients must be within 1 month of initiating or having undergone any type of cancer treatment (i.e., surgery, radiotherapy, chemotherapy) * PATIENT ONLY: Karnofsky performance status (KPS) of 80 or above * PATIENT ONLY: Having a spouse/romantic partner (including same-sex) and who is willing to participate * PATIENT \& PARTNER: Able to read and speak English * PATIENT \& PARTNER: Able to provide informed consent * PATIENT \& PARTNER: Have access to internet connectivity Exclusion Criteria: * PATIENT ONLY: Regularly (self-defined) participation in psychotherapy or a formal cancer support group * PATIENT ONLY: Cognitive deficits that would impede the completion of self-report instruments as deemed by the clinical team
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Glioblastoma are added.
By submitting, you agree to our Terms of use
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
M D Anderson Cancer Center
Houston, Texas, 77030, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can repeated MRI scans reveal how tumors respond to radiation?
- Could dropping one chemo drug improve life for young brain tumor patients?
- Can a RAGE inhibitor tame brain swelling after tumor surgery?
- Can oxygen therapy boost immunotherapy against brain cancer?
- Brain surgery safety: live signal monitoring may shield speech, movement, and sight
- Can new PET scans guide brain tumor catheters more precisely?