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NCT Number: NCT06844370

Home Versus Hospital Based NIV Care in MND

Non-invasive ventilation (NIV) is commonly offered to people with Motor Neurone Disease (MND) who have breathing difficulties. It improves their quality of life and can prolong life by 6 months or more. It is initially used at night and typically set up during a hospital admission. By the time that they develop respiratory failure and need to start NIV, however, most patients require wheelchairs or have other significant health problems. Repeated travel to hospitals is increasingly difficult with increasing disability. It is possible to start and monitor NIV treatment at home. This may be more convenient for selected patients, though starting NIV is quite complex; it is not known if home treatment is as safe and effective as hospital-based treatment.

To establish this, 60 patients with MND who have indications for NIV will be recruited. They will be randomly allocated to a home-based treatment (home NIV set up plus home visits supported by telemonitoring) or hospital-based care (inpatient NIV set up plus outpatient NIV monitoring) and followed up at 1, 4 and 7 months. Alongside measures of treatment effectiveness, assessment of patient and carer preferences, quality of life, and cost-effectiveness will be undertaken.

In the additional qualitative part on this study, interviews with patients who took part in the main study and their carers will be conducted to understand in more depth their perspective on what makes for a good or bad experience with NIV, how the environment (home vs hospital) influences their NIV experience and what personal factors determine NIV use. Findings from the interviews will inform the design of a truly patient-centred NIV service.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Royal Paworth Hospital

Cambridge, CB2 0AY, United Kingdom

Location status: Recruiting

Location contact

Dariusz Wozniak

CONTACT

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults with a diagnosis of Motor Neurone Disease confirmed by a neurologist specialising in MND.
  • Indications to NIV: daytime pCO2 >6.0 kPa or/and symptoms of ventilatory failure (e.g. orthopnoea, paroxysmal nocturnal dyspnoea, morning drowsiness) in the presence of significant diaphragmatic weakness confirmed by respiratory muscle tests

Exclusion criteria

  • Cognitive impairment precluding understanding of the study protocol and valid consent
  • Severe co-morbidities (e.g. decompensated heart failure, severe chronic obstructive pulmonary disease (COPD), morbid obesity) causing or contributing to respiratory failure
  • Immediate need to start NIV (<24hrs) and/or acute illness requiring inpatient treatment e.g. intravenous antibiotics for pneumonia (in addition to the need for NIV)
  • Lack of a sufficient social/professional network to support NIV application at home
  • Not wishing to accept home NIV

Treatment and study plan

Non-invasive ventilation

Other

Providing ventilation support through non-invasive means

Primary outcomes

  1. Control of respiratory failure defined by daytime partial pressure of carbon dioxide (PaCO2)

    Time frame: measured at 1,4,7 months following NIV initiation

    Daytime PaCO2 measured by arterial puncture

  2. Patients and carers experiences of starting and managing NIV, and factors that relate to NIV concordance and acceptance.

    Time frame: measured at 4 weeks since starting NIV

    Semi-structured interview with patients and their carers

Secondary outcomes

  1. NIV acceptance

    Time frame: 1 month

    Percent of patients using NIV for >=4hrs/night

  2. NIV concordance

    Time frame: 1 , 4 and 7 months

    NIV adherence (machine usage in hours/24hours)

  3. Survival

    Time frame: Survival since NIV initiation

    Survival (in months)

  4. Admissions

    Time frame: Up to 7 months from initiation of NIV

    Number of additional planned and emergency hospital admissions

  5. NIV setting changes

    Time frame: 1 , 4 and 7 months

    Number of NIV setting changes required

  6. Cost effectiveness

    Time frame: Up to 7 months from initiation of NIV

    Absolute costs and costs in relation to quality-adjusted life-years (using EQ-5D)

  7. Nocturnal oximetry

    Time frame: 1,4,7 months

    time spent with oxygen saturation <90%(TST90)

  8. Other blood gas analysis measurements of hypoventilation

    Time frame: 1,4,7 months

    Bicarbonate

  9. Quality of life assessment (EQ-5D-5L)

    Time frame: 1,4,7 ,months

    Measurement of quality of life using EQ-5D-5L questionnaire

  10. Quality of life (SRI)

    Time frame: 1,4, 7 months

    Quality of life measured using Severe Respiratory Insufficiency (SRI) questionnaire

  11. Quality of sleep

    Time frame: 1,4,7 ,months

    Sleep quality measured with Pittsburgh Sleep Quality Index (PSQI)

  12. Satisfaction with NIV and healthcare interactions

    Time frame: 7 months

    Satisfaction with NIV and healthcare interactions measured with a visual analogue scale

Study contacts

Contact information is provided by the study sponsor or research team.

Dariusz Wozniak

CONTACT

[email protected]

01223639619

Victoria Stoneman

CONTACT

[email protected]

01223639865

Sponsors and collaborators

Lead sponsor

Papworth Hospital NHS Foundation Trust

Other Gov

Collaborators

  • MND Association
  • University of Nottingham

Registry information

Official study title

Home Initiation and Monitoring of Non-invasive Ventilation (NIV) Versus Hospital-based Care in People with Motor Neurone Disease (MND) : a Randomised Control Trial (RCT) and Qualitative Study

Acronym: HoHoNIV

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Feb 25, 2025
Registry last updated
Feb 25, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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