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The development, implementation and evaluation of the Walk, Talk and Listen over Zoom program for hearing-impaired older adults.

The development, implementation and evaluation of the Walk, Talk and Listen over Zoom program for hearing-impaired older adults.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12622000716763
Acronym
WTL-Zoom
Enrollment
18
Registered
2022-05-18
Start date
2023-01-11
Completion date
2023-09-28
Last updated
2022-05-23

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

Conditions

None listed

Brief summary

Targeted lifestyle interventions that include education, behaviour change and/or group support components could be effective in improving the lifestyle risk factors, increased falls risk and poorer mental health status associated with hearing loss. This study therefore aims to develop, implement and evaluate an online intervention called Walk, Talk and Listen over Zoom (WTL-Zoom). This will be achieved over two phases: 1) a small qualitative study (semi-structured interviews) with older adults with hearing loss to determine the barriers and facilitators to participating in such a program; and 2) applying the findings from phase 1 to inform the development of the WTL-Zoom, followed by a pilot study to evaluate its feasibility and acceptability. Participants for both phases will be primarily recruited from Macquarie University's MQ Health Speech and Hearing Clinic, as well as via university-based advertisements. For the Phase 2 intervention, participants will be divided into subgroups based on their preference of available sessions (morning/afternoon). Sessions will run for 60-minutes once/week over ten-weeks with up to 10 participants per group. Each session including informal socialising and alternating; physical activity with social interaction (PASI) and group auditory rehabilitation (GAR) sessions. In total, there will be five PASI sessions, each running for approximately 30 minutes. These sessions will include mindful breathing, warm-up exercises (e.g., stretching and bodyweight strengthening exercises), moderate-to-vigorous intensity shadow boxing, and cool down exercises (e.g., bodyweight strengthening, balance exercises). There will also be a total of five GAR sessions. These sessions are based on the Ida Institute’s GROUP (Group Rehabilitation Online Utility Pack) program and will run for approximately 30-45 minutes. These sessions will include 1) GAR overview, communication of shared experiences, and goal setting using the Client Oriented Scale of Improvement (COSI) questionnaire; 2) education on understanding hearing loss and impacts on communication; 3) communication strategies: conversational fluency and assertiveness; 4) stress management and personal adjustment; and 5) communication programs and consumer support organisations, review of goals from session 1. A few minutes at the start sessions 2-5 will review the content covered in the previous session.

Interventions

In Phase 1 of this study, the Research Assistant will conduct face-to-face audio-recorded semi-structured interviews with older adults with hearing loss. Participants will primarily recruited from Macquarie University's MQ Speech and Hearing clinic, however other sources of recruitment include flyers posted around the Australian Hearing Hub (Macquarie University), word-of-mouth, and advertisement of the study on the Macquarie University Hearing website and email network. Interviews can be conduc

In Phase 1 of this study, the Research Assistant will conduct face-to-face audio-recorded semi-structured interviews with older adults with hearing loss. Participants will primarily recruited from Macquarie University's MQ Speech and Hearing clinic, however other sources of recruitment include flyers posted around the Australian Hearing Hub (Macquarie University), word-of-mouth, and advertisement of the study on the Macquarie University Hearing website and email network. Interviews can be conducted over-the-phone if preferred. Interviews are expected to last 20-30 minutes and explore the barriers and facilitators to participating in WTL-Zoom. Upon completion of Phase 1, findings from the interviews will be used to inform the adaptation of the WTL-Zoom from the existing WTL program. Once WTL-Zoom has been adapted, participants for Phase 2 will be recruited from the same recruitment sources as Phase 1. The anticipated time between the Phase 2 start date relative to Phase 1 is 2 months. Participants from Phase 1 will also be invited to participate in Phase 2 and if interested, will be provided the Participant Information and Consent Form. Written consent is required before enrolment into Phase 2. A draft form of WTL-Zoom program delivered in Phase 2 will involve the following: Participants will be divided into subgroups based on their preference of available sessions (morning/afternoon). The WTL-Zoom program will be delivered via Zoom. The Research Assistant will contact participants at least 24 hours before their scheduled session with a Zoom link and any other relevant material e.g., activity material that has been specifically designed for this study. The Research Assistant’s phone number will also be provided in case any participant has difficulty accessing Zoom. Sessions will run for up to 60-minutes once/week over ten-weeks in groups of up to 10 participants. Sessions will include informal socialisation, and physical activity with social interaction (PASI) or group auditory rehabilitation (GAR) on alternate weeks. WTL-Zoom will include five PASI sessions that are designed to improve strength, coordination, and balance. The exercises will not require any equipment other than a chair and will be facilitated by the Research Assistant (with an exercise-related qualification) and a research student who will be enrolled in a medical/allied health degree. Each physical activity session will include mindful breathing, warm-up exercises (e.g. stretching and bodyweight strengthening exercises), moderate-to-vigorous intensity shadow boxing, and cool down exercises (e.g. bodyweight strengthening, balance exercises). Exercise intensity will be assessed using the Borg Rating of Perceived Exertion scale. WTL-Zoom will include five GAR sessions that are based on the Ida Institute’s GROUP (Group Rehabilitation Online Utility Pack) program (https://idainstitute.com/tools/group_ar/group_ar_session_plans/). The proposed GAR sessions as part of WTL-Zoom will run for approximately 30-45 minutes and include: 1) GAR overview, communication of shared experiences, and goal setting using the Client Oriented Scale of Improvement (COSI) questionnaire 2); 2) education on understanding hearing loss and impacts on communication; 3) communication strategies: conversational fluency and assertiveness; 4) stress management and personal adjustment; and 5) communication programs and consumer support organisations, review of goals from session 1. A few minutes at the start sessions 2-5 will review the content covered in the previous session.

Sponsors

Macquarie University
Lead SponsorUniversity

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Educational / counselling / training
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Phase 1 (semi-structured interviews) eligibility: 1) aged >= 50 years with any hearing loss, 2) fluent English, 3) consent to participate in the study (including audio recording). Phase 2 (pilot study) eligibility: 1) aged >= 50 years with any hearing loss, 2) fluent English, 3) access to a smart phone, tablet or laptop with a front-facing camera; 4) technical ability to use Zoom or have someone to help; 4) clearance to safely participate in the physical activity components of the intervention (i.e. Physical Activity Readiness Questionnaire (PARQ+) or written physician clearance for participation; 5) written informed consent to participate.

Exclusion criteria

Phase 2 exclusion criteria: 1) unable to ambulate/walk for exercise; 2) serious illness limiting their ability to exercise or complete the trial; 3) contraindications to exercise (i.e. failure to fulfil the prerequisites of the PARQ+); 4) uncontrolled hypertension (>=160/>90 mmHg); 5) signs or symptoms of alcohol/substance abuse and; 6) unable to commit to attending at least 80% of the sessions.

Outcome results

None listed

Source: ANZCTR · Data processed: Aug 31, 2026