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hBET for Pain and Sleep Feasibility

Home-based Brainwave Entrainment Technology (hBET) for Management of Chronic Pain and Sleep Disturbance: A Feasibility Study.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04176861
Enrollment
28
Registered
2019-11-25
Start date
2020-01-20
Completion date
2021-12-31
Last updated
2023-05-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain, Chronic, Sleep Disturbance

Keywords

audio-visual stimulation, brainwave entrainment

Brief summary

Long-term pain affects one-third of the United Kingdom population and can be very disabling. People experiencing long-term pain often suffer from disturbed sleep because of their pain symptoms, and disturbed sleep can then make their pain symptoms worse. Managing long-term pain is also very costly to the National Health Service. The most common treatment is prescribed medicines, but these do not always work and can have serious side-effects for some patients. The investigators have been developing an alternative approach for treating long-term pain. This approach uses simple non-invasive tools to promote some kinds of brain activity over others. It involves patients using headphones to listen to some specific sounds, or a headset with lights flashing at particular frequencies. The studies undertaken so far seem to show that doing this can change how the brain responds to pain. It potentially offers an inexpensive yet effective way of reducing pain and improving sleep for patients with long-term pain. There are a few small studies that support this approach and more work is needed. The next step is to find out whether these tools can be reliably used in home settings, how people feel about using this approach, and to gather information to design a larger trial of this technology. Therefore the aim of this study is to test the suitability and acceptability of these home-based tools with individuals with long-term pain. Up to 30 participants with long-term pain and pain-related sleep disturbance will use the tools for at least 20 minutes at bed time every day for 4 weeks. The investigators will interview them to ask about their experiences of using the tools, and their feedback and suggestions on how the approach should be developed. The investigators will measure changes in the nature of participants' pain, sleep, fatigue and mood. These findings will inform the planning and design of a future much larger study to test this technology. The investigators will make sure that findings from this study are shared widely within the National Health Service and beyond among patient groups, professionals, charities, specialist centres and commissioners.

Interventions

DEVICEhome-based Brainwave Entrainment Technology

Smartphone app-based brainwave entrainment programme using audio stimulation via binaural beats or visual stimulation via flickering lights

Sponsors

University of Leeds
CollaboratorOTHER
University of Manchester
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Chronic non-cancer pain (recurring pain ≥ 3 months duration) * Having nocturnal pain (NRS 0-10 worst pain ≥ 4) * Self-reported sleep difficulties (trouble falling asleep, difficulty staying asleep, waking up too early, or waking up unrefreshed) 3 or more nights per week during the past month

Exclusion criteria

* Planned intervention (injection/ surgery/ new oral medications for pain or sleep) during the 4-week hBET use period * Seizure disorder * Photosensitivity * Hearing or sight problems causing inability to use hBET * Cognitive problems or dementia or mental health disorders causing inability to consent

Design outcomes

Primary

MeasureTime frameDescription
Qualitative semi-structured interviews5 weeksInterview at end of intervention period, following an interview guide, with responses thematically analysed

Secondary

MeasureTime frameDescription
Actigraphy5 weeksMotion watch-based objective measure of gross sleep temporal parameters (total sleep time, sleep latency, wakenings after sleep onset, sleep efficiency)
Brief Pain Inventory5 weeksGives two scores of 0-10 for pain severity and pain interference respectively, with 10 being worst in both cases.
Pittsburgh Sleep Quality Index5 weeksGives a score of 0-21 with higher score indicating worse sleep quality
Sleep and pain diary5 weeksBespoke daily diary recording self reported pain and sleep
Multidimensional Fatigue Inventory5 weeksGives a score of 20-100, with higher scores indicating a higher level of fatigue
EuroQol 5 Dimensions (EQ-5D-5L)5 weeksA measure of global health state, providing a score of 1-5 in each of 5 domains (mobility, self-care, usual activities, pain/discomfort and anxiety/depression), a global index score derived from population references ranging from 0-1 and a self reported description of overall health status on a 0-100 visual-analogue scale
Hospital Anxiety and Depression Scale5 weeksGives two scores of 0-21 for depression and anxiety respectively, with 21 being worst in both cases

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026