Working Memory Training in Adults With ADHD

Attention Deficit Hyperactivity Disorder Clinical Trial

Official title:

Computerised Working Memory Training in Adults With ADHD: A Randomised Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01477125
• Other study ID #: X002
• Secondary ID: DAT-NSPDAT-KV
• Status: Completed
• Phase: N/A
• Start date: November 2013
• Est. completion date: June 15, 2018

Study information

• Verified date: September 2020
• Source: Karolinska Institutet
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate whether computerised working memory training improves cognitive performance, ADHD symptoms, psychosocial functioning and quality of life in adults with ADHD, from psychiatric outpatient clinics (N=100) as well as from a high-security prison facility (N=50).

Description:

The primary aim is to evaluate whether 5 weeks of computerised working memory training improves working memory capacity. Secondary aims are to explore whether improvements in working memory capacity will be transferred to improvements in learning abilities and fluid intelligence. Also, far transfer effects on executive functioning, ADHD symptoms, psychosocial functioning and quality of life will be explored. Finally, it will also be assessed to what extent improvements gained from 5 weeks of working memory training will be maintained 3 and 6 months post-study, respectively.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 102
• Est. completion date: June 15, 2018
• Est. primary completion date: December 15, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Confirmed ADHD according to DSM-IV criteria; ADHD combined type, ADHD inattentive type or ADHD UNS, primarily inattentive type.

• Unmedicated for ADHD during the course of the trial, or being under stable ADHD medication for at least one month at baseline visit and without any planned changes in medication until post-study assessments have taken place.

Exclusion Criteria:

• Previous participation in computerised working memory training (completed training).

• Any psychiatric disorder that in the judgment of the investigator, may interfere with study participation and/or study assessments, also including current substance abuse.

• Participation in psychological treatment addressing ADHD during the course of the 5-week training period (psychoeducation is accepted).

• Initiation of psychological treatment for coexistent disorders during the course of the study (treatment already ongoing at baseline visit is accepted if there are no planned changes during the 5-week training period).

Related Conditions & MeSH terms

• Attention Deficit Disorder with Hyperactivity
• Attention Deficit Hyperactivity Disorder

Intervention

Behavioral:
• Flex working memory training
30-40 minutes of working memory training, 5 days a week for 5 weeks

Locations

Country	Name	City	State
Sweden	Karolinska Institutet	Stockholm

Sponsors (4)

Lead Sponsor	Collaborator
Karolinska Institutet	Stockholm County Council, Sweden, Swedish Prison and Probation Services, The Söderströmska-Königska Foundation

Country where clinical trial is conducted

Sweden, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in a composite measure of working memory capacity	The composite measure of working memory capacity comprises the sum score of: Digit Span score (forwards/backwards); Span Board score (forwards/backwards); Arithmetics score; Spatial Working Memory score	Baseline and 7 weeks
Secondary	Change in a composite measure of working memory capacity	The composite measure of working memory capacity will be assessed in a 6-month follow-up conducted at week 31 post-baseline, equivalent to week 24 post-intervention, to assess retention of any training-related improvements.	Baseline and 31 weeks
Secondary	Change in Digit Span Forwards/Backwards score	Evaluating changes in both Digit Span forwards and backwards scores, as measures of simple verbal working memory capacity.	Baseline, 7 and 31 weeks
Secondary	Change in Span Board Forwards/Backwards score	Evaluating changes in both Span Board forwards and backwards scores as measures of simple visuo-spatial working memory capacity.	Baseline, 7 and 31 weeks
Secondary	Change in Arithmetics score	Evaluating change in Arithmetics score, as a measure of complex verbal working memory capacity as well as of mathematics ability.	Baseline, 7 and 31 weeks
Secondary	Change in Spatial Working Memory score	Evaluating change in Spatial Working Memory score as a measure of complex visuo-spatial working memory capacity.	Baseline, 7 and 31 weeks
Secondary	Change in Qbtest scores	Evaluating changes in Qbtest, a computerised CPT that in addition to measuring inattention and impulsivity also captures motor activity by an IR device during performance of the CPT.	Baseline, 7 and 31 weeks
Secondary	Change in Raven´s Standard Progressive Matrices score	Evaluating change in score of a short version of Raven´s Standard Progressive Matrices, as a measure of fluid intelligence.	Baseline, 7 and 31 weeks
Secondary	Change in Adult ADHD Self-Report Scale (ASRS-v1.1) Symptom Checklist	Evaluating changes in ADHD symptoms by self-reported and informant-reported (significant other) versions of ASRS-v1.1, conducted at baseline, post-intervention, at 3-month and 6-month follow-up.	Baseline, 7, 19, and 31 weeks
Secondary	Change in Sheehan Disability Scale (SDS)	Evaluating changes in psychosocial functioning by the self-reported SDS conducted at baseline, post-intervention, at 3-month and 6-month follow-up.	Baseline, 7, 19, and 31 weeks
Secondary	Change in EuroQol- 5 Dimensions (EQ-5D) questionnaire	Evaluating change in health-related quality of life by the self-reported generic QoL questionnaire EQ-5D, conducted at baseline, post-intervention, at 3-month and 6-month follow-up.	Baseline, 7, 19, and 31 weeks
Secondary	Change in Adult ADHD Quality of Life Measure (AAQoL)	Evaluating change in health-related quality of life by the self-reported ADHD specific QoL measure AAQoL, conducted at baseline, post-intervention, at 3-month and 6-month follow-up.	Baseline, 7, 19, and 31 weeks
Secondary	Montgomery Åsberg Depression Rating Scale-Self report (MADRS-S)	Evaluating if depressive symptoms during the training period, as measured by the self-reported MADRS-S will influence adherence to and results of the working memory training.	Baseline and 7 weeks
Secondary	Adverse events	All adverse events that occurred during the course of the 5-week intervention will be collected as part of the post-intervention assessments at week 7.	Baseline and 7 weeks