Ignite Creation Date:
2024-10-25 @ 7:55 PM
Last Modification Date:
2024-10-26 @ 3:42 PM
Study NCT ID:
NCT06639139
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-10-06
Brief Title:
The Effectiveness of Cognitive-Functional Remote Group Intervention Cog-Fun RG for Adults with Attention Deficit Hyperactivity Disorder ADHD
Sponsor:
None
Organization:
None
Study Overview
Official Title:
The Effectiveness of Cognitive-Functional Remote Group Intervention Cog-Fun RG for Adults with Attention Deficit Hyperactivity Disorder ADHD
Status:
RECRUITING
Status Verified Date:
2024-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
ADHD
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
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
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None