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A pilot study into a role for subvocal speech production in the perception and reduction of AVH

A pilot study into a role for subvocal speech production in the perception and reduction of AVH - Pilot study subvocal speech in AVH

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON55146
Enrollment
50
Registered
2021-05-26
Start date
2021-01-01
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

auditory verbal hallucinations hearing voices

Interventions

The current study aims to investigate whether biofeedback can be used to interrupt AVH perception. Part 1 of the study observes which, if any, sites demonstrate a correlation with EMG activity durin
either the behavioural engagement task is changed or instead of engagement, the relaxation of relevant musculature is trained. The experimenter notes which strategies were successful, how many attem

Sponsors

Rijksuniversiteit Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: In order to be eligible to participate in this study, a subject must meet all of the following criteria: -Able to understand procedures and agree to participate in the study by giving written informed consent -Report having heard voices, measured through the Questionnaire for Psychotic Experiences. And who report that: (1) voices are distinct from thoughts and had a *hearing* quality and (2) voices are experienced daily -Or in the case of control participants, report NOT having heard voices through the Questionnaire for Psychotic Experiences.

Exclusion criteria

Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participation in this study: • Below 18 years of age • IQ below 80 as measured by highest completed education and DART (Dutch adult reading test)

Design outcomes

Primary

MeasureTime frame
The main parameter of the current study is EMG activation during AVH. Study part 1 compares EMG during AVH with baseline (rest) and behavioural tasks (humming, whistling and reading out loud). Study part 2 measures the success of interruption of AVH related EMG activation through behavioural tasks.

Secondary

MeasureTime frame
A secondary study parameter pertains the difference in EMG activation in participants experiencing AVH and a control group who do not experience AVH. This is measured in study 1 by comparing baseline activation patterns and task related EMGs between the AVH+ and AVH- groups.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)