Viewing Study NCT06094400



Ignite Creation Date: 2024-05-06 @ 7:41 PM
Last Modification Date: 2024-10-26 @ 3:11 PM
Study NCT ID: NCT06094400
Status: NOT_YET_RECRUITING
Last Update Posted: 2023-10-23
First Post: 2023-10-17

Brief Title: Pain and Stress Detection and Relief in People With Dementia
Sponsor: The Hong Kong Polytechnic University
Organization: The Hong Kong Polytechnic University

Study Overview

Official Title: Pain and Stress Detection and Relief in People With Dementia Using Portable EEG Headband A Feasibility Study
Status: NOT_YET_RECRUITING
Status Verified Date: 2023-10
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: None
Brief Summary: The objective of this study is to investigate the feasibility and efficacy of using the portable EEG headband and the headband-guided meditation practices for pain and stress relief in people with dementia in Hong Kong Additionally it explores the potential use of the headband as a biomarker for pain and stress in this target group
Detailed Description: This project is a Phase II clinical trial to access the feasibility and efficacy of incorporating portable EEG headband-guided meditation for alleviating pain and stress among people with early and moderate dementia in Hong Kong Sixty dementia people will be recruited Participants in the intervention group will wear the EEG headband and engage in 10-minute guided meditation sessions while the control group will wear the EEG headband and undergo a 10-minute resting session Efficacy will be evaluated using the Wong-Baker Faces Pain Rating Scale Perceived Stress Scale and EEG signals associated with pain and stress Immediate post-assessment focus group interviews will be conducted to explore caregivers experiences with the use of portable EEG headbands in this study

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