Can treating a hidden hormone problem after brain injury restore quality of life?
NCT ID NCT07795736
First seen Aug 31, 2026 · Last updated Sep 01, 2026 · Updated 1 time
Summary
This study looks at adults who had a traumatic brain injury at least a year ago. Researchers want to see whether those with growth hormone deficiency have worse quality of life, fatigue, mood, and sleep than those without it. Participants complete questionnaires and a test for growth hormone deficiency. A subset who are diagnosed with the deficiency and choose treatment will take growth hormone replacement for 12 weeks, with follow-up questionnaires every two weeks.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Growth hormone replacement therapy (for a subset of participants with diagnosed deficiency)
- What this could lead to
- If it works, this could point toward better ways to identify and treat growth hormone deficiency after brain injury, potentially improving quality of life, fatigue, and sleep.
- What could go wrong
- This is an observational study, so it cannot prove cause and effect. The treatment part is small and short, and results may not apply to everyone with TBI.
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.
- Participants
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About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2024
- Expected to finish
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Nov 2028
An estimate. End dates often move.
- Lead sponsor
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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.
Who is studied
Patients who have sustained a traumatic brain injury and have persisting symptoms lasting beyond 1 year post-injury.
- Ages
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18 to 70 years
- Sex
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Anyone
- Healthy volunteers
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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: Adults aged 18-70 years must be referred and have a diagnosis of mTBI made by a brain injury specialist physician and meet the 2023 ACRM diagnostic criteria (Appendix A, Panel A) or the NIH diagnostic criteria for moderate/severe TBI (Appendix A, Panel B). All participants must be symptomatic for at least one-year post-injury (determined by the Glasgow Extended Scale score of less than 8 for moderate/severe TBI and a Rivermead Post-Concussion Questionnaire score of \> 13 with 3 or more symptoms scored \> 3 for mTBI), at the time of screening. All participants must also be fluent in English and be able to either complete questionnaires online or over the phone. In terms of concomitant therapies and medication, all prescription and non-prescription medications (e.g., over-the-counter drugs and herbal supplements) and therapies will be recorded by participants during baseline assessments. Participants with GHD on treatment will be asked to disclose any changes in medications/and or therapies at each bi-weekly follow up questionnaires. Exclusion criteria include untreated pituitary deficits to minimize confounding factors (unless treated/consulted with Dr. Debert and/or Dr. Lithgow), other intracranial abnormalities, chronic neurological conditions, untreated medical conditions, major medical conditions in the past 6 months such as stroke, and current or planned pregnancy.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Foothills Medical Center, Main Floor Special Services
NOT_YET_RECRUITINGCalgary, Alberta, T2N2T9, Canada
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University of Calgary
RECRUITINGCalgary, Alberta, T3G 5N2, Canada
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- MRI tracer could expose hidden brain energy crisis after head injury
- Blood and brain scans may expose invisible injury after head trauma
- Can a handheld scanner find brain bleeds faster on the battlefield?
- A quick eye ultrasound might spot brain pressure without a CT scan
- A new approach to taming Post-TBI fatigue: can group therapy delivered online make a difference?