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Training Listening Skills With the Inclusion of Cognitive Control (TRAILS)

U

Universitaire Ziekenhuizen KU Leuven

Status

Active, not recruiting

Conditions

Hearing Disability

Treatments

Behavioral: Listen training

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Participating in spoken conversation constitutes a multitasking situation with concurrent demands on sensorimotor (auditory, postural) and cognitive functioning (memory, updating, task switching and inhibition). As aging affects multisensory integration and cognitive control, these higher-order processes are likely to put accumulating constraints on listening as adults grow older. By training listening skills (not solely auditory skills), the investigators aim at improving overall communication and quality of life. Moreover, the investigators aim at freeing up cognitive resources in the listen task: the better one gets at a certain domain specific task, the less one needs to draw from other resources and, the more resources are free for another concurrent task. The interdisciplinary approach will inform us about ideal audiological rehabilitation or intervention approaches. Pre-posttests comprise behavioral measures to evaluate listening skills and transfer towards non-trained measures. The training is tablet-based and can be performed at home.

Full description

Goals of the study:

  • Investigate transfer of listening skills to non-trained listening.
  • To develop evidence-based guidelines for clinical audiological rehabilitation.
  • Investigate if the inclusion of cognitive control frees up cognitive resources to use for another concurrent task.
  • Inform about retention following listening training

All participants will be assessed 4 times, with a 4-week interval in between. Participants in the first arm will perform the training during the first two weeks. 4 weeks after training ended and 8 weeks after training ended, retention of training gains will be assessed. Participants in the second arm will perform the delayed training. This is to control for procedural learning effects. After 4 weeks they will start training for 4 weeks. After training retention of training gains will be assessed after 4 weeks. The third arm will start with active control training (listening to stories) for 4 weeks, followed by training for 4 weeks. After these 8 weeks, retention was measured 4 weeks later. Participants are randomly allocated to a group. The efficacy of training will be determined with a within-subject design (i.e. baseline session outcomes will be compared to the final session outcomes of the randomized control trial.

Enrollment

60 patients

Sex

All

Ages

55 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

  • Clients who experience listening and communication difficulties.
  • Clients must not undergo any audiological rehabilitation (auditory training/hearing aid fitting) during the study.
  • Able to operate the training programme as an app on a tablet (e.g. clients have sufficient eyesight to see the exercises; clients must be able to operate the programme).
  • At least 18 years old.
  • Dutch-speaking, as all training material and counselling questions will be presented in Dutch.

Exclusion Criteria (all groups):

  • Severely visually impaired
  • Motorically impaired
  • Cognitively impaired

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 3 patient groups

Immediate training group
Experimental group
Description:
Participants in this group will train immediately for 4 weeks. Afterwards, they will not train for the 8 remaining weeks.
Treatment:
Behavioral: Listen training
Delayed Training Group
Experimental group
Description:
Participants in this group will receive delayed training after 4 weeks of no training.
Treatment:
Behavioral: Listen training
Active control group
Experimental group
Description:
Participants in this group will perform an active control for 4 weeks, followed by 4 weeks of training.
Treatment:
Behavioral: Listen training

Trial contacts and locations

1

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Central trial contact

Astrid van Wieringen, PhD; Mira Van Wilderode, MSc

Data sourced from clinicaltrials.gov

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