The Feasibility of a Brief Attention Training Technique in Improving Behaviour and Attention in Children With ADHD

October 24, 2016 updated by: Adrian Wells, University of Manchester

The Feasibility of a Brief Attention Training Technique for Improving Behaviour and Attention in Children With ADHD

This study aims to investigate the application of the Attention Training Technique in children with ADHD aged 7-11 years old. The research aims to investigate both the feasibility of this technique in this population as well as whether it can improve symptoms, behaviour and executive functioning.

Study Overview

Detailed Description

Attention deficit hyperactivity disorder (ADHD) is a neurobehavioural disorder characterised by core symptoms of hyperactivity, impulsivity and inattention. Its prevalence ranges between 3-9% of school-aged children, making it one of the most common presentations in child and adolescent mental health services.

In the last 10 years, research into the effectiveness of attention training as an intervention for children with ADHD has been increasing. This has tended to follow assumptions that children with the disorder either lack skills in focusing and maintaining their attention and/or have neurological deficits in areas responsible for attention functions. Results have been encouraging, with study participants demonstrating improvements in symptoms and behaviour following a course of attention training. However, the method and length of training has varied across studies.

This study aims to investigate a treatment called the Attention Training Technique (ATT) that approaches attention difficulties in this disorder from a different perspective. Instead of viewing inattention as a result of structural or skills deficits, it posits that children with ADHD have these skills, but are perhaps unaware of the flexibility and control they have over them. This treatment aims to increase this awareness and subsequently improve ratings of attention, behaviour and other areas of executive functioning.

Study Type

Interventional

Enrollment (Actual)

13

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Manchester, United Kingdom, M13 9PL
        • University of Manchester

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

7 years to 11 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Children with a formal diagnosis of ADHD as given by a psychiatrist or community paediatrician
  • Children between the ages of 7 and 11. This age group was selected as previous research on attention training in this population has used this age group
  • Children who are currently on a waiting list at a Child and Adolescent Mental Health Service (CAMHS) or a child psychology service, or being seen by a CAMHS or psychology service for medication review only
  • Children who speak fluent English which will ensure they are able to comprehend the tasks instructions adequately.

Exclusion Criteria:

  • Children who are not stabilised on stimulant medication and/or willing to maintain their medication type/dose
  • Children with a major neurological illness or acquired central nervous system injury
  • Children who at the point of referral have a co-existing diagnosis of an Autistic Spectrum Disorder
  • Children who are currently in receipt of another non-pharmacological intervention for ADHD or who are currently taking part in another research trial

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Attention Training Technique (ATT)
Participants will receive 3-5 sessions of the ATT over a period of 3-5 weeks. A set of standardised instructions will be read to each participant and then they will engage in the procedure for a period of 12 minutes. Participants will listen to a set of auditory stimuli and follow the directions of the recording. This will ask them to focus their attention on selected sounds or spatial locations, switch attention between different sounds and locations, before allocating their attention to all sounds simultaneously. Participants will be given a recording of the ATT on a C.D and asked to practice this at least once before the second session.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Inattention on the Swanson, Nolan and Pelham questionnaire (Snap-IV)
Time Frame: Change from baseline in attention post treatment and at follow up 6 weeks later
Parent's rating of their child's inattentiveness
Change from baseline in attention post treatment and at follow up 6 weeks later

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hyperactivity on the Swanson, Nolan and Pelham questionnaire (Snap-IV)
Time Frame: Change from baseline in hyperactivity post treatment and at follow up 6 weeks later
Parent's rating of their child's hyperactivity
Change from baseline in hyperactivity post treatment and at follow up 6 weeks later
Impulsivity on the Swanson, Nolan and Pelham questionnaire (Snap-IV)
Time Frame: Change from baseline in impulsivity post treatment and at follow up 6 weeks later
Parent's rating of their child's impulsivity
Change from baseline in impulsivity post treatment and at follow up 6 weeks later
Attentional control on the Attentional Control Scale for Children (ASC-C)
Time Frame: Change from baseline in attentional control post treatment and at follow up 6 weeks later
Children's self reported ability to focus and shift their attention
Change from baseline in attentional control post treatment and at follow up 6 weeks later
Behaviour on the Strengths and Difficulties Questionnaire (SDQ)
Time Frame: Change from baseline in behaviour post treatment and at follow up 6 weeks later
Parent's ratings of their child's behaviours
Change from baseline in behaviour post treatment and at follow up 6 weeks later
Executive functioning on The Behavioural Rating Inventory of Executive Functioning (BRIEF)
Time Frame: Change from baseline in executive functioning post treatment and at follow up 6 weeks later
Parent's ratings of their child's executive functioning behaviours in the home environment
Change from baseline in executive functioning post treatment and at follow up 6 weeks later
Working memory on the Weschler Intelligence Scale for Children (WISC-IV) - Digit Span
Time Frame: Change from baseline in working memory post treatment and at follow up 6 weeks later
Children's Working memory as assessed by the Digit Span subtest
Change from baseline in working memory post treatment and at follow up 6 weeks later
Working memory on the Weschler Intelligence Scale for Children (WISC-IV) - Letter Number Sequencing
Time Frame: Change from baseline in working memory post treatment and at follow up 6 weeks later
Children's Working memory as assessed by the Letter Number Sequencing subtest
Change from baseline in working memory post treatment and at follow up 6 weeks later
Treatment Acceptability Questionnaire
Time Frame: Rated once at the final session of treatment, 4 weeks after the 2nd baseline is taken
Parents rating of the acceptability of the treatment
Rated once at the final session of treatment, 4 weeks after the 2nd baseline is taken

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Adrian Wells, University of Manchester

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

August 1, 2015

Primary Completion (Actual)

May 1, 2016

Study Completion (Actual)

May 1, 2016

Study Registration Dates

First Submitted

July 31, 2015

First Submitted That Met QC Criteria

August 3, 2015

First Posted (Estimate)

August 6, 2015

Study Record Updates

Last Update Posted (Estimate)

October 25, 2016

Last Update Submitted That Met QC Criteria

October 24, 2016

Last Verified

October 1, 2016

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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