Acquired brain injury Nervous System Diseases
Conditions
Interventions
Baseline assessment
All participants at the baseline stage will complete questionnaires online with the study Research Support Fellow. Questionnaires will assess well-being, mood, anxiety, suicide ris
Sponsors
University of Nottingham
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: 1. Acquired brain injury experienced as an adult (>18 years), at least 3 months prior to joining the study 2. Age >18 years 3. Self-reported sense of being ‘stuck’ and/or emotional difficulties related to ABI rehabilitation (screened during initial interview) 4. English-speaking 5. Able to access the online platform 6. Ability to give informed consent and complete outcome measures
Exclusion criteria
Exclusion criteria: 1. Pre-existing intellectual disability 2. Severe psychiatric disorder (at time of screening or in previous year), and/or factors (e.g., suicidal intent or ideation) indicating alternative treatment may take priority 3. Comorbid neurodegenerative condition 4. Indication that group intervention may not be appropriate (screened during baseline and initial interview)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Mood/Depression measured using Patient Health Questionnaire 9 at baseline, and 2-weeks post intervention completion. 2. Risk of suicide using the Columbia Suicide Severity Rating Scale at baseline, and 2-weeks post intervention completion. 3. Anxiety using the Generalised Anxiety Scale-7 at baseline, and 2-weeks post intervention completion. 4. Acceptance using the Acceptance and Action Questionnaire at baseline, and 2-weeks post intervention completion. 5. Living towards values using the Valued Living Questionnaire at baseline, and 2-weeks post intervention completion. 6. Self-compassion using the Self-Compassion questionnaire at baseline, and 2-weeks post intervention completion. 7. Cognition using the ACE-III (mini) at baseline, and 2-weeks post intervention completion. 8. Goal attainment using the GAS-Lite at baseline, and 2-weeks post intervention completion. 9. Quality of life measured using the QOLIBRI at baseline, and 2-weeks post intervention completion (awaiting confirmation from ethics as submitted as an amendment) | — |
Secondary
| Measure | Time frame |
|---|---|
| There are no secondary outcome measures | — |
Countries
England, United Kingdom
Outcome results
None listed