Hypnosis in Working Memory Rehabilitation

Releasing Residual Cognitive Capacity After Acquired Brain Injury: A Randomized Controlled Trial Using Hypnotic Suggestion in Rehabilitation of Working Memory

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.

Study Overview

• Status: Recruiting
• Conditions: Brain Injuries; Cognitive Impairment; Working Memory; Cognitive Rehabilitation
• Intervention / Treatment: Other: Hypnotic suggestion; Other: Mindfulness

Detailed Description

The potential impact of applying hypnosis in cognitive rehabilitation is substantial. Deficits in WM is one of the most common challenges after ABI and plays a critical role in post-injury outcome. Still, state-of-the-art approaches within WM rehabilitation have not been able to produce significant effects that transfer to real- life functioning for the affected patients. Building on the strong results of hypnosis on WM in ABI from a Danish single trial, we will aim at replication and expansion of the study in a Norwegian context. The initial study will be expanded in terms of number of participants, injury-characteristics will be included, outcome measures of relevance to real-life functioning, and underlying mechanisms of change will be explored. Self-efficacy is generalizable by nature (self-efficacy gained from mastery experiences in one situation generalizes to others), thus WM rehabilitation effects are expected to generalize and transfer to other domains in daily life.

This randomized controlled trial (RCT) aims to evaluate the effectiveness of hypnosis in WM rehabilitation in ABI patients. Ninety patients will be recruited from Sunnaas Rehabilitation Hospital. Inclusion criteria are non-progressive ABI, minimum 12 months post- injury, ongoing WM deficits and age between 18 and 67 years. Patients will be randomized to either a) an intervention group receiving four weekly 60 min. sessions with induction and hypnosis, b) an active control group receiving four weekly 60 min. sessions of induction and mindfulness, or c) a passive control group without intervention. The targeted procedure consists of suggestions about enhancing WM functions through the instantiation of preinjury WM ability in the present using age regression and visualizations of brain plasticity. The non- targeted suggestions contain no explicit mentioning of ABI or WM-related abilities. Each participant will be assessed at baseline, immediately after intervention and six months after baseline. Primary outcome is WM as measured by neuropsychological tests as well as self- and informant reported WM capacity. Secondary outcomes include self-rated ABI related symptoms, self-efficacy, mental health, and global outcome. A process evaluation will be carried out to evaluate treatment experience,

Rehabilitation of impaired WM after ABI has hitherto yielded limited clinical effects, and clinical trials of new interventions are thus warranted. Long-standing empirical evidence demonstrates that hypnosis is an effective therapeutic technique in a wide range of conditions, including in altering cognitive functions and improving WM in healthy adults, supported by imaging data. Recent exploratory research has suggested remarkable efficacy of hypnosis in improving WM in patients with ABI. However, these findings need replication in studies applying scientifically rigorous designs. If successful, our ambition is to provide recommendations and materials to implement hypnotic suggestion as an adjunct treatment following ABI in Norwegian rehabilitation clinics. Study findings may inform future studies exploring the use of clinical hypnosis in other areas of rehabilitation, such as mild TBI, and in other neurological conditions where WM deficit is prominent.

• Study Type: Interventional
• Enrollment (Anticipated): 90
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Marianne Løvstad, Profesor; Phone Number: +4793452003; Email: Marianne.Lovstad@sunnaas.no
• Study Contact Backup: Name: Line Sophie Eide, Cand.psyc; Phone Number: +4797950051; Email: Line.Eide@sunnaas.no

Study Locations

• Norway
  • Viken
    • Nesoddtangen, Viken, Norway, 1453
      • Recruiting
      • Sunnaas rehabilitation hospital
      • Contact: Anne Catrine Martinsen, PhD; Email: anne.catrine.traegde.martinsen@sunnaas.no

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 67 years (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

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

Study Plan

How is the study designed?

Design Details

• Primary Purpose: TREATMENT
• Allocation: RANDOMIZED
• Interventional Model: PARALLEL
• Masking: DOUBLE

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
EXPERIMENTAL: Hypnotic suggestion; During the first phase of the study, two groups will receive identical hypnotic inductions followed by targeted suggestion for one group and non-targeted suggestion for the other. The targeted procedure consists of suggestions about enhancing WM functions through the instantiation of preinjury WM ability in the present using age regression and visualizations of brain plasticity.	Other: Hypnotic suggestion; The intervention group will receive four weekly 60 min. sessions with hypnosis treatment including induction followed by hypnotic suggestion.
ACTIVE_COMPARATOR: Mindfulness; The targeted procedure consists of suggestions about enhancing WM functions through the instantiation of preinjury WM ability in the present using age regression and visualizations of brain plasticity.	Other: Mindfulness; The active control group will receive four weekly 60 min. sessions of induction and mindfulness-based instructions.
NO_INTERVENTION: No treatment; The passive control group receives no intervention

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in WM on neuropsychological tests	Measured by the WM Index WAIS IV	Change from Baseline (T1) to immediately after the intervention period (T2) and 8 months after Baseline (T3)
Change in WM-related symptoms in everyday life	Assessed with the WM subscale from the Behavior Rating Inventory of Executive functioning Adult version (BRIEF-A) on a 3-point scale: Never a problem, sometimes a problem or often a problem. Higher scaled score indicates higher level of problems with WM.	Change from Baseline (T1) to immediately after the intervention period (T2) and 8 months after Baseline (T3)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in cognitive composite score as seen on neuropsychological tests	Measured by Trail Making A+B, D-KEFS CWIT 1-4, CVLT-II, WAIS IV Digit Symbol	Change from Baseline (T1) to immediately after the intervention period (T2) and 8 months after Baseline (T3)
Change in TBI related challenges in everyday life	Measured by the Patient Competency Rating Scale on a 5-point scale from 1 can't do it to 5: No problem to do it. Higher total scaled score represents better every day functioning.	Change from Baseline (T1) to immediately after the intervention period (T2) and 8 months after Baseline (T3)
Change in self reported mental health	Measured with the Hopkins Symptom Checklist (HSCL) on a scale from 1 (not at all) to 4 (a lot). Higher mean score reflects a higher level of emotional distress.	Change from Baseline (T1) to immediately after the intervention period (T2) and 8 months after Baseline (T3)
Change in quality of life	Assessed with Quality of Life After Brain Injury (QOLIBRI) on a satisfaction scale from 0 (not satisfied) to 5 (very satisfied). Higher satisfaction indicates higher quality of life.	Change from Baseline (T1) to immediately after the intervention period (T2) and 8 months after Baseline (T3)
Changes in community integration	Assesed with Participation Assessment with Recombines Tools-Objective (PART-O) on a 5-point scale: None, 1-4 hours, 5-9 hours, 10-19 hours, 20-34 hours, 35 hours or more. Higher mean scaled score indicates better community integration.	Change from Baseline (T1) to immediately after the intervention period (T2) and 8 months after Baseline (T3)

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
Changes in ABI related self-efficacy	The tool to measure Traumatic Brain Injury Self-Efficacy is rated on a scale from 0 (very uncertain) to 10 (Very certain). Higher total score on the questionnaire indicates higher TBI related self-efficacy.	Change from Baseline (T1) to immediately after the intervention period (T2) and 8 months after Baseline (T3)
Changes in WM self-efficacy	The Memory Self-Efficacy Questionnaire (MSEQ) is rated on a scale from 0 (never) to 12 (100% of the time). Higher total scales score indicates higher WM self-efficacy.	Change from Baseline (T1) to immediately after the intervention period (T2) and 8 months after Baseline (T3)

Collaborators and Investigators

• Sponsor: Sunnaas Rehabilitation Hospital
• Collaborators: University of Oslo
• Investigators: Principal Investigator: Marianne Løvstad, Profesor, Sunnaas Rehabilitation Hospital and University of Oslo

Study record dates

Study Major Dates

• Study Start (ACTUAL): August 15, 2022
• Primary Completion (ANTICIPATED): April 1, 2024
• Study Completion (ANTICIPATED): April 1, 2024

Study Registration Dates

• First Submitted: March 9, 2022
• First Submitted That Met QC Criteria: March 9, 2022
• First Posted (ACTUAL): March 18, 2022

Study Record Updates

• Last Update Posted (ACTUAL): November 8, 2022
• Last Update Submitted That Met QC Criteria: November 7, 2022
• Last Verified: November 1, 2022

More Information

Terms related to this study

• Keywords: Rehabilitation; Self-efficacy; Randomized controlled trial (RCT); Clinical Hypnosis; Aquired brain injury
• Additional Relevant MeSH Terms: Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Wounds and Injuries; Craniocerebral Trauma; Trauma, Nervous System; Brain Injuries; Physiological Effects of Drugs; Central Nervous System Depressants; Hypnotics and Sedatives
• Other Study ID Numbers: Hypnoseprosjektet

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No