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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

Prof Rod Taylor
+44 (0)141 353 7500
Rod.Taylor@glasgow.ac.uk


Mrs Emma Burrell
+44 (0)141 330 4744
REACH-HFpEFproject@glasgowctu.org


More information about this study, what is involved and how to take part can be found on the study website.

Study Location:

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Be Part of Research - Trial Details - Trial of a facilitated home-based rehabilitation intervention in patients with heart failure

Trial of a facilitated home-based rehabilitation intervention in patients with heart failure

Medical Conditions

Exercise-based cardiac rehabilitation in patients with heart failure with preserved ejection fraction (HFpEF).


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


Cardiac rehabilitation (CR) is a highly effective and cost-effective treatment for people with heart failure and is the recommended NHS treatment. It improves quality of life and may reduce risk of a hospital admission. However, at present less than one in 20 people in the UK discharged from hospital with diagnosis of heart failure participate in CR. A key reason for this is that people with heart failure find it difficult to get to hospital, and some dislike group formats. With the COVID-19 pandemic, the barrier to accessing hospital based cardiac rehabilitation programmes has become much greater.

Between 2012-18, the trial team co-developed and tested (with people with heart failure, clinicians, and National Health Service (NHS) managers) a home-based CR programme called ‘Rehabilitation EnAblement in CHronic Heart Failure (REACH-HF)’. Through a clinical trial, they were able to confirm that participation in REACH-HF improves quality of life of people with heart failure with reduced ejection fraction (‘HFrEF’) and that it is affordable for the NHS. They now wish to carry out a study to assess that REACH-HF also works for people with heart failure with preserved ejection fraction (‘HFpEF’).

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

25 May 2022 31 May 2025

Participants who consent to take part will be involved with the study for about twelve months. They will firstly be invited by their local cardiology/heart failure research team to take part in an initial assessment to check that they are suitable to participate in the study and, if so, to complete some questionnaires. If this is a face-to-face meeting, they will also be asked to undertake a walking test and provide a sample of blood. Once the initial assessment is completed, they will then be allocated at random (like tossing a coin) to either the REACH-HF programme plus usual care or usual care only.

For participants assigned to the REACH-HF programme plus usual care group:
They will be contacted by one of the clinical team (usually a CR nurse, HF specialist nurse, physiotherapist) to set up a phone call, online appointment, or home visit (if available) to start participants on the 12-week REACH-HF programme.

The facilitator will help participants to: develop skills for managing heart failure; make plans about how to improve their current situation; monitor their progress over time, and adapt their heart failure management strategies if necessary. More details are available on the REACH-HF website (http://sites.exeter.ac.uk/reach-hf/).

A small group of participants and their caregivers who participate in the REACH-HF programme will be asked to take part in an interview at 4 and 12 months to talk about their experience in receiving the intervention and ways in which it can be improved.

For participants assigned to the usual care group:
They will continue to receive usual care for their heart failure as per their local and national guidelines.

All participants will be asked to repeat the walking test, questionnaires and provide a blood sample at the 4 and 12 months visits.

As part of the study, participants will be asked to wear an activity monitor. This is a wrist-worn ‘watch’ which records all their movements throughout the day as well as their sleep patterns; participants will be asked to wear it for 24 hours a day, for 9 consecutive days. The monitor is waterproof and can be worn at all times; therefore, there should be no need for it to be removed. Participants will receive instructions on how and where to attach the monitor. All participants will be asked to do this at the start of the study then again at 4 and 12 months. The monitor cannot be used to locate anyone and does not transmit any live data while wearing it. All the movement data is stored on the watch.


Adults aged 18 years or over with HFpEF and their caregivers.

You can take part if:



You may not be able to take part if:


Current participant exclusion criteria as of 03/04/2024:1. Patients who have undertaken CR within the last 12 months2. Patients who have any contraindications to exercise training (according to local cardiac rehabilitation guidelines)3. Probable alternative diagnoses that in the opinion of the investigator could account for the patient’s HF symptoms (i.e. dyspneoa, fatigue), such as significant pulmonary disease (including primary pulmonary hypertension), anaemia, or obesity. Specifically, patients with the following should be excluded:3.1. Severe pulmonary disease including COPD (i.e. requiring home oxygen, chronic nebulizer therapy, or chronic oral steroid therapy or hospitalised for pulmonary decompensation within 12 months)3.2. Haemoglobin <10 g/dll3.3. BMI >40 kg/m²;4. Patients with prior ejection fraction <45%.5. Patients located in a long-term care home/support setting who are considered to be too frail to engage with the intervention or who are unwilling to travel to research assessments or accommodate home visits.6. Patients who are unable to understand the study information or unable to complete the outcome questionnaires.7. Patients judged to be unable to participate in the study for any other reason (e.g. psychiatric disorder, diagnosis of dementia, life-threatening co-morbidity).



Previous participant exclusion criteria:1. Patients who have undertaken CR within the last 12 months2. Patients who have any contraindications to exercise training3. Patients who have alternative reasons for shortness of breath such as significant pulmonary disease or severe COPD, haemoglobin <10 g/dl, or body mass index (BMI) >40 kg/m²4. Patients with prior ejection fraction <45%5. eGFR <30 ml/min


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Cambridge University Hospitals NHS Foundation Trust
    Cambridge Biomedical Campus Hills Road
    Cambridge
    CB2 0QQ
  • Royal Gwent Hospital
    Cardiff Road
    Newport
    NP20 2UB
  • Royal Free London NHS Foundation Trust
    Royal Free Hospital Pond Street
    London
    NW3 2QG
  • York Hospital
    York Teaching Hospital NHS Foundation Trust Wigginton Road
    York
    YO31 8HE
  • St Thomas' Hospital
    Guy's and St Thomas' NHS Foundation Trust Westminster Bridge Road
    London
    SE1 7EH
  • Darlington Memorial Hospital
    County Durham and Darlington NHS Foundation Trust Hollyhurst Road
    Darlington
    DL3 6HX
  • Aintree University Hospital
    Liverpool University Hospitals NHS Foundation Trust Lower Lane
    Liverpool
    L9 7AL
  • Ninewells Hospital and Medical School
    NHS Tayside Department of Cardiology
    Dundee
    DD1 9SY
  • Glasgow Royal Infirmary
    NHS Greater Glasgow and Clyde 84 Castle Street
    Glasgow
    G4 0SF
  • Lister Centre
    NHS Ayrshire and Arran University Hospital Crosshouse
    Kilmarnock
    KA2 0BE
  • Kings College Hospital NHS Foundation Trust
    Denmark Hill
    London
    SE5 9RS
  • Glenfield Hospital
    Leicestershire Partnership NHS Trust Groby Road
    Leicester
    LE39 9QP
  • Manchester Royal Infirmary
    Manchester Heart Centre Manchester University NHS Foundation Trust Oxford Road
    Manchester
    M13 9WL
  • University Hospital of North Tees
    North Tees and Hartlepool NHS Foundation Trust Hardwick Road
    Stockton on Tees
    TS19 8PE
  • Royal Devon and Exeter Hospital
    Cardiology Department Royal Devon and Exeter NHS Foundation Trust Barrack Road
    Exeter
    EX2 5DW
  • Russell's Hall Hospital
    The Dudley Group NHS Foundation Trust Pensnett Road
    Dudley
    DY1 2HQ
  • West Suffolk Hospital
    The Cardiac Centre West Suffolk NHS Foundation Trust Hardwick Lane
    Bury Saint Edmunds
    IP33 2QZ
  • St Catherine's Health Centre
    Wirral Community Health and Care NHS Foundation Trust Derby Road Tranmere Wirral
    Merseyside
    CH42 7HA
  • Wycombe Hospital
    Cardiology Research Ward 3B Buckinghamshire Healthcare NHS Trust
    Wycombe
    HP11 2TT
  • John Radcliffe Liaison Office
    John Radcliffe Hospital Headley Way Headington
    Oxford
    OX3 9DU

It is hoped that participation in REACH-HF will improve how participants feel and how they are able to manage their heart failure. The information provided from this study will help the research team to understand how to best make home cardiac rehabilitation available for people with heart failure.
It is not expected for participants to be harmed in any way by taking part in this study. Cardiac rehabilitation for people with heart failure has been shown to be safe. As Cardiac rehabilitation involves exercise, there is always a risk that participants might initially have muscle soreness. The facilitator will make sure that the starting level of exercise is appropriate for the participant. Whilst working through some of the sections of the REACH-HF Manual with the facilitator, participants may be asked questions about their experiences with heart failure and its impact on day-to-day life which might be upsetting. The facilitators are trained health professionals and will ask questions sensitively, and participants don’t have to answer any questions which cause them to feel upset. The facilitator can refer participants to their heart failure and cardiology service or GP for further support.

Mrs Emma Burrell
+44 (0)141 330 4744
REACH-HFpEFproject@glasgowctu.org


Prof Rod Taylor
+44 (0)141 353 7500
Rod.Taylor@glasgow.ac.uk



More information about this study, what is involved and how to take part can be found on the study website.


The study is sponsored by NHS Greater Glasgow and Clyde and funded by Health Technology Assessment Programme.




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Read full details for Trial ID: ISRCTN47894539
Last updated 11 November 2024

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