Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06895824

Somatic Tracking for Tinnitus

Led by University College London Hospitals · Updated on 2025-03-26

100

Participants Needed

1

Research Sites

20 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

We are examining the effect of mindfulness meditation on attitudes towards tinnitus, as well as physical and psychological distress associated with the condition. The meditation is designed to promote neuroplasticity, fostering new neural connections to help you reinterpret tinnitus through a lens of safety and reduce the perception of threat. This approach integrates several techniques from various psychological therapies which have been promising in reducing tinnitusrelated distress. Therefore, the purpose of this study is to see whether a guided mindfulness meditation intervention is effective in improving the acceptance of tinnitus symptoms, as well as reducing tinnitus-related distress in people living with tinnitus.

CONDITIONS

Official Title

Somatic Tracking for Tinnitus

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Experiencing distressing tinnitus
  • Sufficient English language and hearing ability to take part
  • Completed all relevant medical and audiological investigations and concluded ensuing treatment for any underlying disease
  • Not be engaging in any other therapy for tinnitus.
Not Eligible

You will not qualify if you...

  • Risk to self (scoring 'nearly every day' on PHQ-9 question "Thoughts that you would be better off dead, or of hurting yourself in some way?")
  • Severe mental health difficulties (PHQ-9 score of 20 or more)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Online

London, United Kingdom, NW1 9UT

Actively Recruiting

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Research Team

F

Florian Vogt

CONTACT

S

Shyn Wei Phua

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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