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Clinical Trials/NCT06639139
NCT06639139RecruitingNot Applicable

The Effectiveness of Cognitive-Functional Remote Group Intervention (Cog-Fun RG) for Adults with Attention Deficit Hyperactivity Disorder (ADHD)

Hebrew University of Jerusalem1 site in 1 country40 target enrollmentStarted: November 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
40
Locations
1
Primary Endpoint
The adult ADHD quality of life scale

Study Overview

Brief Summary

The goal of this clinical trial is to examine the effectiveness of Cognitive-Functional Remote Group intervention (Cog-Fun RG).

The main questions of this study are 1. will participants demonstrate improvements in their executive functioning and quality of life after receiving the intervention, compared to waitlist controls. In addition, the investigators will examine if the waitlist group will demonstrate similar gains in these outcomes after receiving the same intervention.

the investigators will compare between the intervention group to the waiting list group to examine the effect of the intervention.

The participants will be allocated into two groups: an intervention group and a waiting list group.

The intervention group will receive the the Cog-Fun RG intervention, which includes 21 weekly group sessions, each lasting 90 minutes. the participants will be required to complete questionnaires at several time points: pre-post the intervention, as well as three months, six months, and one year after the intervention.

The waiting list controls will be required to complete questionnaires at several time points: pre-post waiting period, and then after the intervention, as well as three months, six months, and one year after the intervention.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Crossover
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • * Self Reported ADHD diagnoses

Exclusion Criteria

  • * Self Reported other major health condition that impedes daily functioning

Outcomes

Primary Outcomes

The adult ADHD quality of life scale

Time Frame: at baseline, immediately after the intervention, immediately after the waiting period and 3 months after the intervention follow up

Questionnaire with 29 questions relating to productivity, life outlook, relationships and psychological health. each question is rated on a 5 point scale. Raw scores are transformed to a 1-100 scale. higher scores indicate higher quality of life. The assessment will be conducted at baseline, immediately after the intervention, immediately after the waiting period and 3 months after the intervention follow up.

Secondary Outcomes

  • Behavioral Rating Inventory of Executive Functions (BRIEF) Adult Self -Report(at baseline, immediately after the intervention, immediately after the waiting period.)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Adina Maeir

Prof. Adina Maeir, School of Occupational Therapy, Hebrew University

Hebrew University of Jerusalem

Study Sites (1)

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