Skip to content

Pain and Stress Detection and Relief in People With Dementia

Unknown statusNot applicableNCT06094400
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

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.

Study details

Official title
Pain and Stress Detection and Relief in People With Dementia Using Portable EEG Headband: A Feasibility Study
Conditions
Interventions
Sponsor
The Hong Kong Polytechnic University
Start date
2023-10-17
Primary completion
2024-06-30
Sex
All
Age range
from 18 Years
Results posted
No results posted in this snapshot
Total sites listed
0

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * People with mild to moderate severe dementia; * Have chronic pain or have experienced stress for at least six months; * Be able to communicate and express pain; * Have no prior experience with any type of meditation training; * Volunteer to participate in the study and provide written informed consent Exclusion Criteria: * Person with other acute or terminal illnesses that may not be able to stay in a home living environment frequently; * With severe visual or hearing problems that would hinder communication; * With infectious diseases that could be transmitted by using the headband.

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06094400