Training Listening Skills With the Inclusion of Cognitive Control — TRAILS  

Hearing Disability Clinical Trial

Official title: Training Listening Skills With the Inclusion of Cognitive Control

Status Active, not recruiting

Clinical Trial Summary

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.

Clinical Trial 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. ;

Related Conditions & MeSH terms

• Hearing Disability

• NCT number: NCT05766020
• Study type: Interventional
• Source: Universitaire Ziekenhuizen KU Leuven
• Status: Active, not recruiting
• Phase: N/A
• Start date: April 3, 2023
• Completion date: June 30, 2024