Cognitive-Functional Remote Group Intervention for Adults with ADHD
The Effectiveness of Cognitive-Functional Remote Group Intervention (Cog-Fun RG) for Adults with Attention Deficit Hyperactivity Disorder (ADHD)
This study is testing a new online group program to see if it can help adults with ADHD improve their thinking skills and overall quality of life.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years to 60 Years |
| Sex | All |
| Sponsor | Hebrew University of Jerusalem Academic / other |
| Locations | 1 site (Jerusalem) |
| Trial ID | NCT06639139 on ClinicalTrials.gov |
What this trial studies
This clinical trial investigates the effectiveness of a Cognitive-Functional Remote Group intervention (Cog-Fun RG) aimed at improving executive functioning and quality of life in adults diagnosed with ADHD. Participants will be divided into an intervention group, which will attend 21 weekly group sessions, and a waitlist control group. The study will assess changes in outcomes through questionnaires administered before and after the intervention, as well as at three and six months post-intervention. The goal is to determine whether the intervention leads to significant improvements compared to the waitlist group.
Who should consider this trial
Good fit: Ideal candidates for this study are adults who have self-reported diagnoses of ADHD.
Not a fit: Patients with other major health conditions that impede daily functioning may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could enhance executive functioning and overall quality of life for adults with ADHD.
How similar studies have performed: While similar approaches have been explored, this specific intervention's effectiveness remains to be fully validated.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: \* Self Reported ADHD diagnoses Exclusion Criteria: \* Self Reported other major health condition that impedes daily functioning
Where this trial is running
Jerusalem
- Hebrew University — Jerusalem, Israel (Recruiting)
Study contacts
- Study coordinator: Adina Prof. Maeir, PhD
- Email: adina.maeir@mail.hui.ac.il
- Phone: 972 546205081
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.