NCT02516917

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
13

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Aug 2015

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 31, 2015

Completed
1 day until next milestone

Study Start

First participant enrolled

August 1, 2015

Completed
5 days until next milestone

First Posted

Study publicly available on registry

August 6, 2015

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2016

Completed
Last Updated

October 25, 2016

Status Verified

October 1, 2016

Enrollment Period

9 months

First QC Date

July 31, 2015

Last Update Submit

October 24, 2016

Conditions

Outcome Measures

Primary Outcomes (1)

  • Inattention on the Swanson, Nolan and Pelham questionnaire (Snap-IV)

    Parent's rating of their child's inattentiveness

    Change from baseline in attention post treatment and at follow up 6 weeks later

Secondary Outcomes (8)

  • Hyperactivity on the Swanson, Nolan and Pelham questionnaire (Snap-IV)

    Change from baseline in hyperactivity post treatment and at follow up 6 weeks later

  • Impulsivity on the Swanson, Nolan and Pelham questionnaire (Snap-IV)

    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)

    Change from baseline in attentional control post treatment and at follow up 6 weeks later

  • Behaviour on the Strengths and Difficulties Questionnaire (SDQ)

    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)

    Change from baseline in executive functioning post treatment and at follow up 6 weeks later

  • +3 more secondary outcomes

Study Arms (1)

Attention Training Technique (ATT)

EXPERIMENTAL

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.

Behavioral: Attention Training Technique

Interventions

Attention Training Technique (ATT)

Eligibility Criteria

Age7 Years - 11 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

  • 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.

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Manchester

Manchester, M13 9PL, United Kingdom

Location

MeSH Terms

Conditions

Attention Deficit Disorder with Hyperactivity

Condition Hierarchy (Ancestors)

Attention Deficit and Disruptive Behavior DisordersNeurodevelopmental DisordersMental Disorders

Study Officials

  • Adrian Wells

    University of Manchester

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor of Clinical and Experimental Psychopathology

Study Record Dates

First Submitted

July 31, 2015

First Posted

August 6, 2015

Study Start

August 1, 2015

Primary Completion

May 1, 2016

Study Completion

May 1, 2016

Last Updated

October 25, 2016

Record last verified: 2016-10

Data Sharing

IPD Sharing
Will not share

Locations