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Telehealth in Motor Neurone Disease

Telehealth in Motor Neurone Disease: A Single Centre, Randomised Controlled Feasibility and Pilot Study of the Use of the TiM Telehealth System to Deliver Highly Specialised Care in Motor Neurone Disease at a Distance

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02464748
Acronym
TiM
Enrollment
77
Registered
2015-06-08
Start date
2014-09-01
Completion date
2016-04-01
Last updated
2026-05-19

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

Conditions

Motor Neuron Disease

Brief summary

Motor neurone disease (MND) is a rare but debilitating neurological condition that causes paralysis of the body's muscles leading to severe disability and eventually death. Patients often struggle to travel the long distances to specialist clinics to receive the care they require whilst this expert care is often unavailable in the community. Telehealth has the potential to enable a specialist team to monitor the health and wellbeing of patients and their carers whilst they are at home. This could improve the patient's health, improve the quality of life of both patients and their carers, and lead to more effective use of health resources. This is a randomised controlled pilot study that will involve 40 patients who are cared for by the Sheffield Motor Neurone Disease care centre and their main informal carer (a total of 80 participants). Half of the participants will use the telehealth system for a minimum of six months and maximum of eighteen months and information will be collected from patients, carers and their care team. This will include collecting clinical outcome measures, health resource use and the opinions and experience of using the system. All participants will continue to receive their usual care. This is a pilot study. It aims to determine the feasibility and acceptability of the telehealth system to patients, carers and their health care providers. It also aims to determine how a larger trial could successfully evaluate the clinical and cost-effectiveness of the system.

Detailed description

MND is often referred to as amyotrophic lateral sclerosis (ALS) or Lou Gehrig's disease.

Interventions

OTHERTiM telehealth arm

Sponsors

Sheffield Teaching Hospitals NHS Foundation Trust
Lead SponsorOTHER
University of Sheffield
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

Patient Inclusion Criteria: * Patients aged 18 years or over who have attended the MND clinic at the Royal Hallamshire Hospital, Sheffield. * Patients with amyotrophic lateral sclerosis diagnosed by a consultant neurologist with symptom onset within the last three years. o Or * Patients with amyotrophic lateral sclerosis, primary muscular atrophy or progressive lateral sclerosis diagnosed by a consultant neurologist with a deterioration in their condition as evidenced by a deterioration in the ALS functional rating score (ALSFRS-R) by at least two points during the previous 18 months. * Live within 120 minute drive from Sheffield Patient

Exclusion criteria

* Patients attend another MND care centre in the UK. * Significant impairment in decision making capacity preventing informed consent by the subject due to a major mental disorder including fronto-temporal dementia. * Patient unable to use the TiM system due to physical, intellectual or language difficulties and unwilling to permit carer to operate it on their behalf. Patients will be asked to complete two questions used within the TiM system, with, or without the help to their carer to verify their ability to use the system. * The patient has no eligible informal carer willing to participate in the trial * Insufficient mobile telephone reception in the patients' home to use the TiM system. * Any other major impairment that may affect their ability to participate in the study Carer inclusion criteria * Age 18 years or older * Person identified by the patient as the major provider of informal care (emotional and/or practical support) to the patient and provides more than one hour per week of unpaid care * Carer willing to allow data they provide during the trial to be shared by the research team with their own doctor in the event of serious clinical need. Carer

Design outcomes

Primary

MeasureTime frameDescription
Feasibility and acceptability of using the telehealth system from interviewsUp to 18 monthsRecruitment rate, retention rate.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 20, 2026