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NCT Number: NCT06018103

MBCT-vision VSS RCT

Visual Snow Syndrome (VSS) is a neurological condition with bran network dysregulation involving the visual pathway. This is a research trial comparing the effect of an 8-week mindfulness-based intervention via a group-learning course, the MBCT-vision programme, to treat Visual Snow Syndrome, compared to people on a standard care (wait-list control). Participants will be randomly allocated to either the Treatment group (MBCT-vision), or the Control group (wait-list control). After a waiting period, people allocated to the Control group will also be offered the MBCT-vision treatment. The primary outcome is to compare the severity of the visual symptoms on a 0 to 10 scale between the two groups.

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Key information

Age range

16 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

Visual Snow Syndrome (VSS) is a neurological condition where affected people see flickering dots across their whole visual field, & may have other symptoms such as light sensitivity, after-images, trailing of images, & tinnitus. Functional Magnetic Resonance Imaging (fMRI) studies in VSS have shown brain network dysregulation involving the visual pathway. There is currently no evidence-based validated treatment for VSS, therefore the current standard of care is no treatment.

This research trial is to test the treatment of an intensive mindfulness programme, using the Mindfulness Based Cognitive Therapy customised for visual symptoms (MBCT-vision) programme, for people with Visual Snow Syndrome. MBCT-vision is a group learning programme, where people meet once weekly for 8 weeks. During these once weekly sessions, they learn mindfulness practices. The group discussions about the mindfulness practices introduces cognitive behavioural skills. Participants are given daily home practices between these weekly group learning sessions. We completed a study (ClinicalTrials.gov identifier NCT04184726) showing MBCT-vision was a feasible treatment for VSS.

This clinical trial is a 'randomized controlled trial'(RCT), where the effectiveness of a treatment is evaluated by comparison between two groups. We are recruiting people with VSS. Participants will be randomly allocated to one of two groups: one group receives MBCT-vision; while another group received standard care only for 5 months. The second group is called a waiting-list control group, whereby after 5 months, they will receive MBCT-vision treatment. The study will be conducted from single centre at a tertiary care hospital and the MBCT-vision is delivered online.

The key outcome of interest is severity of Visual Snow Syndrome on a 0-10 visual analogue scale. Other outcome measures will be collected to understand the effect of MBCT-vision, including quality of life and psychological wellbeing.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • People with VSS according to the ICHD-3 criteria; previously diagnosed by a Neurologist, Ophthalmologist or Neuro-Ophthalmologist

Exclusion criteria

  • Patients with co-morbid conditions affecting vision
  • Patients with a current severe depressive or psychotic episode as determined by the psychologist
  • Patients with severe difficulties in emotional regulation as determined by the psychologist
  • Patients unable to provide informed consent for participation
  • Patients with insufficient understanding of spoken English (due to need to participate in group discussions)
  • Patients who have previously completed MBCT or similar mindfulness interventions
  • Persons aged <16 or >80 years

An exploratory sub-study on the change in metabolomics will recruit healthy controls, inclusion criteria:

Healthy Control Inclusion Criteria

  • Family or household member of a similar age (+/- 8years) to a participant with VSS recruited into the MBCT-vision VSS RCT study
  • Person with no symptoms of VSS
  • Person who self-declares as fit and well with no current medical conditions including anxiety or migraine

Healthy Control Exclusion Criteria

  • Person unable to provide informed consent
  • Person with other co-morbid medical or psychological conditions
  • Person aged <16 or >80years

Treatment and study plan

MBCT-vision

Behavioral

8-week mindfulness group learning course, using Mindfulness Based Cognitive Therapy customised for visual symptoms (MBCT-vision). Participants meet once weekly only, with daily home practice between sessions.

Primary outcomes

  1. Severity of visual symptoms of Visual Snow Syndrome on a 0-10 VAS

    Time frame: 5 months

    Severity of VSS visual symptoms

Secondary outcomes

  1. Psychological wellbeing on the World Health Organisation (WHO) wellbeing index scores

    Time frame: 5 months

    WHO-5 wellbeing index

  2. Psychological distress on the Clinical Outcomes in Routine Evaluation (CORE-10) scores

    Time frame: 5-months

    CORE-10 scores

  3. Impact of Visual Snow Syndrome symptoms on daily life on 0-10 scale

    Time frame: 5-months

    VSS impact

  4. Work and Social Adjustment Scale

    Time frame: 5-months

    impact of VSS on work and social function

Study contacts

Contact information is provided by the study sponsor or research team.

Abigail Orr

CONTACT

[email protected]

020 7188 4885

Sui Wong, MD

CONTACT

[email protected]

020 7188 4885

Sponsors and collaborators

Lead sponsor

Guy's and St Thomas' NHS Foundation Trust

Other

Registry information

Official study title

MBCT-vision to Treat Visual Snow Syndrome: a Randomized Controlled Trial

Important dates

Study start
2024
Primary completion
2025
Study completion
2026
First posted
Aug 30, 2023
Registry last updated
Aug 31, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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