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Auditory Rehabilitation in Stroke Patients With Auditory Processing Disorders

University College London (UCL) logo

University College London (UCL)

Status

Completed

Conditions

Stroke
Auditory Processing Disorder, Central

Treatments

Other: personal frequency modulated systems

Study type

Interventional

Funder types

Other

Identifiers

NCT02889107
11/LO/1675

Details and patient eligibility

About

This study aimed to evaluate long term benefits in speech reception in noise, after daily 10 week use of an assisting listening device (personal frequency-modulates systems) , in non-aphasic stroke patients with auditory processing deficits.

Full description

Stroke can affect all levels of the auditory pathway. Approximately one in five stroke survivors report severe difficulties when listening to speech-in-noise, despite normal hearing, attributed to abnormal processing of sounds within the brain, and these individuals are more likely to experience communication difficulties in poor acoustic environments, The patient with significant auditory deficits and functional limitations may require a range of rehabilitation and remediation approaches. Several studies conclusively demonstrate substantial improvements in speech recognition in noise when using personal frequency-modulated (FM) systems. These devices are used to improve speech perception in noise in adults with neurological disorders including stroke with good immediate benefits. However, the long-term benefits of FM systems in stroke patients has not been studies. In this research study the investigators aimed to investigate the long term benefits in speech reception in noise in non-aphasic stroke patients and measure the potential improvement in unaided speech in background noise performance after 10 weeks.

Enrollment

9 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Clinical history of ischaemic stroke verified by brain magnetic resonance imaging (MRI)
  • Diagnosis of auditory processing disorders
  • Normal pure-tone audiogram

Exclusion criteria

  • Severe aphasia
  • Significant psychiatric illnesses

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

9 participants in 2 patient groups

standard care
No Intervention group
Description:
Patients received standard listening strategies for 10 weeks
intervention
Experimental group
Description:
Patients received an assistive listening device (personal frequency modulated systems) for 10 weeks
Treatment:
Other: personal frequency modulated systems

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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