Clinical Trials Directory

Trials / Unknown

UnknownNCT06094400

Pain and Stress Detection and Relief in People With Dementia

Pain and Stress Detection and Relief in People With Dementia Using Portable EEG Headband: A Feasibility Study

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
The Hong Kong Polytechnic University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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 caregiver's experiences with the use of portable EEG headbands in this study.

Conditions

Interventions

TypeNameDescription
OTHERMeditationParticipants in the intervention group will be furnished with a tablet incorporating a pre-installed Muse Meditation App and a set of headphones. They can choose their preferred immersive soundscape for the meditation session.
OTHERControlParticipants allocated to the control group will similarly wear the portable EEG headband, but they will receive a rest session without any additional intervention

Timeline

Start date
2023-10-17
Primary completion
2024-06-30
Completion
2024-06-30
First posted
2023-10-23
Last updated
2023-10-23

Source: ClinicalTrials.gov record NCT06094400. Inclusion in this directory is not an endorsement.