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Clinical Trials/NCT02220140
NCT02220140UnknownNot Applicable

Resilience for Young People With Attention Deficit Hyperactivity Disorder (ADHD) - a Randomized Controlled Trial of a Brief Intervention Program.

University of Aarhus1 site in 1 country8,000 target enrollmentStarted: August 1, 2014Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
8,000
Locations
1
Primary Endpoint
Adult ADHD Self-Report Scale (ASRS-v1.1)

Study Overview

Brief Summary

In this project we invite 8.000 young persons (age 18-27) in Denmark and to participate in a randomized controlled intervention study where we aim to test the effectiveness of a web based knowledge and inspiration program about resilience for children, adolescents and adults (called myresilience.org). The complete CONSORT trial protocol is available at http://myresilience.org/ at the subsite 'about us'.

Detailed Description

The complete CONSORT trial protocol is available at http://myresilience.org/ at the subsite 'about us'.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 27 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •A random sample with 8.000 patients registered in the Danish National Patient Register:
  • •Age 18-27
  • •ADHD diagnosis

Exclusion Criteria

  • •Request for legal protection against contacts from researchers.

Arms & Interventions

Control

No Intervention

Service as usual

Intervention group

Experimental

Participants are offered access to the web based resilience program and are invited to join a short introduction course.

Intervention: The Resilience Program (Behavioral)

Outcomes

Primary Outcomes

Adult ADHD Self-Report Scale (ASRS-v1.1)

Time Frame: Follow-up will be on the average 1 year after intervention

The Symptom Checklist is an instrument consisting of the eighteen Diagnostic and Statistical Manual criteria (DSM-IV). Six of the eighteen questions were found to be the most predictive of symptoms consistent with ADHD. These six questions are the basis for the ASRS v1.1. The measure is a number score. The ASRS-v1.1 will be administered to all participants before and 1 year after the intervention.

Secondary Outcomes

  • The 12-item General Health Questionnaire (GHQ-12)(Follow-up will be on the average 1 year after intervention)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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