Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03231488
Other study ID # IRAS project ID: 213205
Secondary ID
Status Recruiting
Phase N/A
First received July 24, 2017
Last updated August 9, 2017
Start date July 31, 2017
Est. completion date January 2018

Study information

Verified date June 2017
Source University of East Anglia
Contact Katrina Vicentijevic
Phone 07498045055
Email k.vicentijevic@uea.ac.uk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Can mindfulness help with attention and emotion difficulties after a brain injury?

People who have a brain injury often have problems with their attention and emotions. This study will see if a short mindfulness task can help with these problems. So far, there are not many studies looking at this and those that do show mixed results. When being mindful someone is aware of their attention and focuses on the present moment without passing judgement. This study focuses on over-selectivity and selective attention to threat after a brain injury. These are two concepts involved in attention and emotion problems. Over-selectivity is when someone focuses on only one thing around them and misses other key things. Selective attention to threat is when someone's focus is drawn to something around them that is seen as threatening. This has been shown to cause and keep anxious feelings going. This research will see if a short mindfulness task can help those with a brain injury by reducing overselectivity and selective attention to threat on two tasks. Participants will be recruited from NHS and non-NHS brain injury services. The study will take around two hours to complete for each participant. In summary, this study looks to see if a specific mindfulness exercise can be helpful for specific attention and emotion problems. It could be a first step in making treatment better and giving more treatment options for those with a brain injury.


Recruitment information / eligibility

Status Recruiting
Enrollment 46
Est. completion date January 2018
Est. primary completion date January 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Aged 18 years and over

- Medical evidence of ABI with attention or executive functioning difficulties, such as difficulties with planning, inhibition or attention

- Time since ABI to be 9 months or greater • ABI severity to be moderate to severe, determined by the Mayo classification system (Malec et al., 2007). This is classification system is frequently used to determine ABI severity and is standard practice to record at the acute stage of care when the individual is admitted to hospital. This means there must be evidence of one or more of the following in medical notes: the individual's lowest Glasgow Coma Scale (GCS) score is less than 13, there is a loss of consciousness of at least 30 minutes immediately following ABI and post traumatic amnesia (PTA) is at least 24 hours in length. If there is no evidence of this in the medical notes, then there must be evidence that the individual has clinically significant difficulties resulting from their ABI to have needed a referral to brain injury services.

- There are self-reported or clinician-identified emotional difficulties to adjusting to circumstances post-ABI

Exclusion Criteria:

- Significant, severe and enduring presence of mental health difficulties or substance misuse that would prevent valid engagement in experimental tasks

- Perceptual, language, communication, reading or motor difficulties that would prevent valid engagement in experimental tasks

- The presence of developmental or acquired dyslexia affecting the automatic reading of words in the emotional Stroop

- Severe cognitive difficulties that would prevent valid engagement in experimental tasks

- Presence of pre-existing or comorbid disorders that may affect cognitive functioning (other than ABI) that would prevent valid engagement in experimental tasks

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Mindfulness intervention
A 10 minute mindfulness of breath exercise
Control intervention (unfocused attention)
A 10 minute unfocused attention intervention - participants are asked to let their mind wander on anything that comes to mind.

Locations

Country Name City State
United Kingdom Cambridge University Hospitals Nhs Foundation Trust Cambridge
United Kingdom Cambridgeshire Community Services Nhs Trust Cambridge
United Kingdom Headway Cambridgeshire Cambridge
United Kingdom Brain Injury Rehabilitation Trust Ely
United Kingdom Headway Essex Essex
United Kingdom Headway Norfolk & Waveney Norfolk
United Kingdom Norfolk Community Health and Care Nhs Trust Norfolk
United Kingdom Northamptonshire Healthcare Nhs Foundation Trust Northampton
United Kingdom Partnerships in Care Northampton
United Kingdom St Andrews Healthcare Northampton
United Kingdom Cambridgeshire and Peterborough Nhs Foundation Trust Peterborough
United Kingdom Icanho, Livability Stowmarket

Sponsors (13)

Lead Sponsor Collaborator
University of East Anglia Brain Injury Rehabilitation Trust, Cambridge University Hospitals NHS Foundation Trust, Cambridgeshire and Peterborough NHS Foundation Trust, CAMBRIDGESHIRE COMMUNITY SERVICES NHS TRUST, Headway Cambridgeshire, Headway Essex, Headway Norfolk and Waveney, Icanho, Livability, NORFOLK COMMUNITY HEALTH AND CARE NHS TRUST, NORTHAMPTONSHIRE HEALTHCARE NHS FOUNDATION TRUST, Partnerships in Care, St Andrews Healthcare

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Emotional Stroop This will be a computer task that measures selective attention to threat.
In the emotional Stroop, different coloured words are presented to participants and the emotional meaning of the words are manipulated. Participants are instructed to name the colour of the words as quickly as possible, whilst ignoring the meaning of the words. Selective attention to threat will be inferred when word colour-naming takes longer when the meaning of the word is threatening relative to neutral. So, the greater the difference between reaction times to neutral and threatening words, the greater the selective attention to threat.
Administered pre- and post- 10-minute intervention, so over a period of one hour
Primary Over-selectivity task. This will be a computer task that measures over-selectivity.
Practice phase - two cards, each with two images appear on the screen. One card is the correct one to select and the other is incorrect. This happens for two sets of two cards (pair 1 and pair 2). Test phase - participants are presented with two single stimuli simultaneously, one from the reinforced compound and one from the verbally punished compound (Figure 4). They are instructed to select one of the pictures on the screen.
Over-selectivity will occur if participants fail to learn about one of the stimuli in the previously reinforced compound and therefore fail to select that stimuli they had not learned about in the practice phase.
So, the higher the score on the over-selectivity task, the greater the difference between the most and least chosen stimuli, which means that the participant is demonstrating greater over-selectivity.
Administered pre- and post- 10-minute intervention, so over a period of one hour
Secondary Hospital Anxiety and Depression Scale (HADS) A self-report measure consisting of 14 items. The measure gives an overall score, as well as separate scores for severity of anxiety and depression subscales. Pre-intervention (baseline measure)
Secondary The Five Facet Mindfulness Questionnaire (FFMQ) This will be used to characterise levels of mindfulness. This is a self-report measure, consisting of 39 items. Pre-intervention (baseline measure)
Secondary Test of Everyday Attention (TEA) Subtests will be used to measure baseline measures of attention. Elevator counting is a measure of sustained attention and elevator counting with distraction is a measure of selective attention. Pre-intervention (baseline measure)
Secondary Weschler Test of Adult Reading (WTAR) This will be used to measure a baseline measure of pre-morbid functioning. Participants read a list of 50 words with irregular pronunciations to assess previous learning of the words. Pre-intervention (baseline measure)