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A clinical trial of a telehealth work support program for stroke survivors

A multisite, single-blind, parallel-group randomised controlled trial of a telehealth work support program versus usual care for adults with stroke

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12626000646347
Acronym
The RESET Trial
Enrollment
194
Registered
2026-05-28
Start date
2026-09-02
Completion date
2029-01-30
Last updated
2026-09-07

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

Conditions

None listed

Brief summary

Failure to provide vocational support after stroke costs Australia $3.6 billion in lost productivity yearly. Vocational support in Australia is limited to return to work (RTW) support in some rehabilitation services. This results in significant service gaps, particularly in rural and remote communities. We have co-developed a telehealth post-stroke Work Support Program designed to ensure vocational support needs are met any time throughout the RTW and long term work participation journey. We will conduct a randomised controlled trial comparing the Work Support Program to usual care to determine if the program results in a significantly greater improvement in work ability. We will recruit 194 stroke survivors across Australia, collecting work ability and other vocational and wellbeing outcomes by telephone at baseline, 3, 6 and 12-months post baseline; evaluate cost efficacy, and conduct a process evaluation to examine factors that will impact on translation.

Interventions

Arm 1: Work Support Program (WSP) The Work Support Program is a telehealth-delivered, individualised work support intervention for adults who have had a stroke. The program is delivered individually by trained Work Support Program Clinicians (health professionals) via telephone or videoconference. The WSP is guided by a facilitator manual based on pilot work and designed specifically for this trial. The program has four mandated sessions (assessment sessions and discharge), with the remaining

Arm 1: Work Support Program (WSP) The Work Support Program is a telehealth-delivered, individualised work support intervention for adults who have had a stroke. The program is delivered individually by trained Work Support Program Clinicians (health professionals) via telephone or videoconference. The WSP is guided by a facilitator manual based on pilot work and designed specifically for this trial. The program has four mandated sessions (assessment sessions and discharge), with the remaining sessions guided by the participants individual goals and needs. The intervention includes: • Having a WSP Clinician for up 6-months. • Three specialised assessment sessions (up to 1 hour each or split across shorter sessions if required) that enable identification of gaps in care, barriers and facilitators to work, and an individualised Workplace Action Plan. • This WSP Clinician will identify gaps in current supports/care; identify and facilitate referrals; and communicate with care providers/workplaces/support people as appropriate (and with permission) to ensure the participant is accessing appropriate supports/services. • For those returning to work, the WSP Clinician will participate in development of a Return to Work Plan, and delivery of that plan, including liaison with workplaces (with permission). • For those who are unemployed, the WSP Clinician will support liaison with disability employment services and assist in identifying and applying for potential jobs. Additional strategies (CV review; interview practice; role plays and so on) will be implemented as required. • For those currently working, the WSP Clinician will support the participant in following their Workplace Action Plan, with revisions to the plan as new barriers emerge. This may include liaison with the workplace as required (with permission). • Additional support around enhancing work-life balance will be provided as appropriate (psychoeducation, identification of barriers and strategy identification/goal setting). WSP clinicians will also be trained in supporting emotional adjustment to stroke, person centred goal setting and problem solving. • A discharge plan at the end of the intervention delivery. Training: WSP Clinicians will undergo structured training prior to delivery, including a minimum of 4 hours of online videos/reading; 3 hours of face to face training, and 3 hours of role plays prior to the first participant enrolment; followed by regular individual/group supervision and fidelity checks during study delivery. Duration & Frequency: Up to 6 months post-enrolment. Frequency of sessions and number of sessions are not pre-specified, but will be agreed upon by the WSP Clinician and participant, based on their needs and goals. Session length will also vary depending on session content (approx. 15 minutes to 1 hour maximum). There are four mandated sessions, as such “per protocol” will be defined as a minimum of 4 sessions attended. Mode: Telehealth (telephone or videoconference), delivered individually. Delivered by: Trained Work Support Program clinicians (registered health professionals with at least 2 years clinical experience). Fidelity: Clinical notes will be coded and audited. For fidelity analysis, Work Support Program Clinicians will digitally record the sessions (with client’s permission). On an ongoing basis an independent fidelity assessor will review audio recordings for 10% of randomly selected participants, rating against a checklist of expected activities according to the manual for percentage adherence, with any barriers to delivery and new/additional strategies not currently in the manual noted.

Sponsors

Deakin University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Investigator, Outcomes Assessor)

Eligibility

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

Inclusion criteria

(1) Aged 18+ (2) Residing in Australia (3) Diagnosed with stroke (including ICD-11 diagnoses (or equivalent, depending on local coding systems) of Intracerebral haemorrhage, Subarachnoid haemorrhage, Cerebral ischemic stroke, or Stroke not known if ischaemic or haemorrhagic) at any time, confirmed by imaging (4) Meet criteria of employment before stroke (work for average of =7 hours/week, including planned or sick leave, during the month prior to the stroke for pay/profit/commission/in-kind or in a family business) (5) Have access to a phone (6) Willing to provide contact details for their treating physician (7) Willing to provide contact details for follow-up (8) Can provide informed consent

Exclusion criteria

(1) Not currently interested in engaging with or able to participate in a telehealth program targeting work ability and delivered in English, or not currently eligible to work in Australia (2) Have been working at the same job for 60 days or more (post-stroke) and currently have good work ability (Work Ability Index score >=37) (3) Currently enrolled in a compensable RTW program (e.g. WorkCover) or enrolled in a clinical trial judged not to be scientifically or medically compatible with this study

Outcome results

None listed

Source: ANZCTR · Data processed: Sep 19, 2026