Hypnosis in Working Memory Rehabilitation (NCT05287542) | Clinical Trial Compass
CompletedNot Applicable
Hypnosis in Working Memory Rehabilitation
Norway90 participantsStarted 2022-12-15
Plain-language summary
Establishment of effective, efficient, and evidence-based interventions in rehabilitation of working memory (WM) deficits after acquired brain injury (ABI) is sorely needed. Despite robust evidence for the usefulness of clinical hypnosis in a wide range of clinical conditions, and improved understanding of mechanisms underlying it ́s effects, the potential of clinical hypnosis in cognitive rehabilitation is virtually unexplored. The current study seeks to replicate resent intriguing findings where large effects of hypnotic suggestion were seen on WM capacity following ABI, and further, explore underlying mechanisms of change.
Who can participate
Age range
18 Years – 67 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* A documented non-progressive ABI, minimum 12 months post- injury and ongoing WM deficits by self-report and/or neuropsychological assessment
* The above mentioned patients have received multidisciplinary cognitive rehabilitation before participation
Exclusion Criteria:
* Patients with severe mental illness
* Patients progressive neurologic disease
* Patients with ongoing ICD-10 diagnosis of substance dependence
* Patients that lack Norwegian language skills
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1This trial used hypnosis as part of working memory rehabilitation — is that an approach that makes sense for my specific type of brain injury or cognitive impairment, and is there any evidence it worked better than standard cognitive rehab techniques?
2Since this trial is already completed, would my doctor be able to access any published results or data showing whether hypnosis actually improved working memory on neuropsychological tests or helped people function better in daily life?
3The trial measured changes in everyday working memory symptoms, not just test scores — based on my current difficulties at home or work, does my doctor think that kind of outcome would be meaningful for me compared to other rehabilitation options already available?
4Because this study was Phase NA, meaning it was likely exploratory or feasibility-focused, does that mean there's still a lot unknown about the safety and effectiveness of hypnosis-based cognitive rehab, and should I consider a more established treatment first?
5Are there other completed or ongoing trials, or standard-of-care cognitive rehabilitation programs, that my doctor would recommend comparing against this hypnosis-based approach before deciding on a treatment path?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Change in WM on neuropsychological tests
Timeframe: Change from Baseline (T1) to immediately after the intervention period (T2) and 6 months after Baseline (T3)
2
Change in WM-related symptoms in everyday life
Timeframe: Change from Baseline (T1) to immediately after the intervention period (T2) and 6 months after Baseline (T3)