Viewing Study NCT04726813



Ignite Creation Date: 2024-05-06 @ 3:41 PM
Last Modification Date: 2024-10-26 @ 1:55 PM
Study NCT ID: NCT04726813
Status: COMPLETED
Last Update Posted: 2022-06-15
First Post: 2021-01-08

Brief Title: An Internet-delivered Intervention for Coping With ADHD in Adulthood
Sponsor: University of Bergen
Organization: University of Bergen

Study Overview

Official Title: An Internet-delivered Intervention for Coping With ADHD in Adulthood - a Randomized Controlled Trial
Status: COMPLETED
Status Verified Date: 2022-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: MyADHD
Brief Summary: The primary aim of this study is to examine the efficacy of a self-guided Internet-delivered intervention for coping with ADHD The secondary aim is to investigate the effects of individual adaptation of the intervention on adherence satisfaction and clinical outcomes
Detailed Description: ADHD in adulthood with an estimated prevalence of 2 - 3 is associated with challenges in daily life functioning The availability of evidence-based psychological interventions for adults with ADHD is poor Interventions delivered over the Internet might help to increase the availability of effective psychological interventions for this group The primary aim of this study is to examine the efficacy of a self-guided Internet-delivered intervention for coping with ADHD The secondary aim is to investigate the effects of individual adaptation of the intervention on adherence satisfaction and clinical outcomes A minimum of 118 participants with a self-reported ADHD diagnosis will be included in the study In phase 1 we will conduct a randomized controlled trial with two arms 1 self-guided Internet-delivered intervention for coping with ADHD N59 2 self-guided online psychoeducation control group N 59 with a 3 month follow-up After 3 months the second phase of the study starts In this phase II the control group participants will receive an adaptive version of the Internet-delivered intervention This includes adaptation of the order of the modules to the individual participant needs with the use of rule-based and machine-learning based adaptation Clinical outcomes in both phases are inattention hyperactivity quality of life and stress Uptake usage adherence and satisfaction will be explored Repeated measurers are at baseline weekly during the intervention period post-intervention and 3 months follow-up

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None