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Task Training In Older Adults With Age-Related Hearing Loss

P

Pamukkale University

Status

Completed

Conditions

Age Related Hearing Loss
Physical Disability
Vestibular Disease
Hearing Loss

Treatments

Other: TASK TRAINING

Study type

Interventional

Funder types

Other

Identifiers

NCT05190081
60116787-020/1933.

Details and patient eligibility

About

This study aimed to examine the effects of single and dual-task training on physical function, cognitive function, quality of life, balance, concerns about falling, and activities of daily living in the elderly with age-related hearing loss.

The elderly who were diagnosed with age-related hearing loss in Pamukkale University Health, Practice and Research Center, Department of Otorhinolaryngology participated in the study. The elderly were allocated a single-task training group, dual-task training group, and control group. Thirteen patients in the single-task training group, 15 patients in the dual-task training group, 14 patients in the control group completed the study. Degrees of hearing loss were determined by pure tone audiometry. Evaluations, Senior Fitness Test, Montreal Cognitive Assessment, World Health Organization- Quality of Life- Old Module, Berg Balance Scale, Falls Efficacy Scale International, Functional Independence Measure, Dual Task Questionnaire, Dual Task Effect, were performed initially, after the interventions and at the 6th month. The interventions were carried out two days a week and 40 minutes, for five weeks.

Full description

Outcome Measures Physical function, cognitive function, auditory function, quality of life, balance, concerns about falling, independence in activities of daily living, and dual-task performance were evaluated. Older adults were evaluated initially, after the dual-task and single-task training, and at 6th month for long-term control. All evaluations and interventions were carried out in an isolated and quiet environment in the examination room of the Department of Otorhinolaryngology.

Interventions A special program including motor and cognitive tasks was prepared. Both lower and upper extremity motor tasks and verbal, arithmetic, auditory, and visual cognitive tasks were planned based on evidence. Tasks were completed at the same time in the dual-task training group, were completed separately in the single-task training group. No intervention was performed in the control group. The dual-task and single-task training were held 2 days a week, 40 minutes, for a total of 10 sessions for 5 weeks. A patient-appropriate task was selected for each cognitive task each week. It has been tried to prevent the learning effect by providing individual and weekly progress according to the patients' performance in the tasks in the motor and cognitive parts. Variable priority instructions were used in the dual-task training group, and fixed priority instructions were used in the single-task training group. At the beginning and end of the intervention programs, 7 types of warm-up and cool-down exercises involving large muscle groups were performed for 10-minutes. Each task in the intervention programs was performed for 60 seconds and/or 10 repetitions.

Enrollment

43 patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Being >65 years old
  • Montreal Cognitive Assessment Scale score > 21
  • Diagnosed with Age-Related Hearing Loss
  • Having bilateral symmetrical hearing loss (average ±10dB difference)
  • Having normal visual functions
  • Ability to ambulate independently (may use a self-help device)

Exclusion criteria

  • Using a hearing aid
  • Receiving a physical therapy intervention for Age-Related Hearing Loss
  • Having an orthopedic or neurological condition that may affect cognition or postural control
  • Using medication that may affect cognition or postural control
  • Having vertigo or being hospitalized in the emergency room due to vertigo attacks
  • Missing or refusing the follow-up

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

43 participants in 3 patient groups

single-task training group
Experimental group
Description:
Tasks were completed separately in the single-task training group
Treatment:
Other: TASK TRAINING
dual-task training group
Experimental group
Description:
Tasks were completed at the same time in the dual-task training group
Treatment:
Other: TASK TRAINING
control group
No Intervention group
Description:
No intervention was performed in the control group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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