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Internet-delivered ACT for Treating the Psychological Effects of Hearing Loss

Internet-delivered ACT for Treating the Psychological Effects of Hearing Loss

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02877329
Enrollment
58
Registered
2016-08-24
Start date
2014-02-28
Completion date
2015-05-31
Last updated
2016-08-24

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

Conditions

Hearing Loss

Keywords

psychological effects

Brief summary

Randomized trial comparing internet-delivered ACT with therapist support against waiting list for persons with hearing loss and comorbid psychological distress

Detailed description

Hearing loss is the most common sensory disability in the world. Hearing loss is an auditory disability which affects not only speech recognition, but also the ability to recognize, locate and identify sounds in one's environment. Today there are a variety of studies investigating the relationship between hearing loss and mental health. For example, there are studies showing that hearing loss can lead to depression, somatization, social isolation, worrying or anxiety, loneliness, smaller social networks, lower self-efficacy, sensitivity to stress, burnout, and impaired sleep quality and quality of life in comparison with people with normal hearing. Initial results from other studies indicate that acceptance may be of importance, as it in turn can lead to increased help-seeking.To avoid prolonged stress and a healthy self-efficacy could contribute to greater well-being of people with hearing loss. This is the first study to use ACT to improve psychological health in people with hearing loss through the process of psychological flexibility. The treatment is eight weeks long and internet delivered through self-help texts with weekly therapist support.

Interventions

BEHAVIORALInternet-delivered ACT

Therapist-guided Internet-delivered ACT (acceptance and commitment therapy) for 8 weeks

Sponsors

Linkoeping University
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 110 Years
Healthy volunteers
No

Inclusion criteria

* HHIE-S score over 8 * Indication of comorbid psychological suffering/distress (defined as total score above 0 on PHQ9/GAD7 or below 1sd on QOLI)

Exclusion criteria

* No computer with internet connection * Unability to understand written content * Incomplete screening procedure * A health condition that needs immediate care

Design outcomes

Primary

MeasureTime frame
The Hearing Handicap Inventory for Elderly-Screening, change between pre and post treatmentthrough study completion, an average of 8 weeks

Secondary

MeasureTime frame
Generalized Anxiety Disorder 7 (GAD7), change between pre and post treatmentthrough study completion, an average of 8 weeks
Quality of Life Inventory (QOLI), change between pre and post treatmentthrough study completion, an average of 8 weeks
Patient Health Questionnaire Depression 9 (PHQ9), change between pre and post treatmentthrough study completion, an average of 8 weeks
Hearing Self-Efficacy (HSE), change between pre and post treatmentthrough study completion, an average of 8 weeks
Perceived Stress Scale-4 (PSS-4), change between pre and post treatmentthrough study completion, an average of 8 weeks
Hearing Acceptance Questionnaire (HAQ), change between pre and post treatmentthrough study completion, an average of 8 weeks

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026