Comparison of Traditional, Web-based or a Combined Cardiac Rehabilitation Programme

Sponsor
University of Chester (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05326529
Collaborator
University Hospital of Derby and Burton NHS Foundation Trust (Other)
45
1
3
3.6
12.5

Study Details

Study Description

Brief Summary

The study explores the different modes of Cardiac Rehabilitation delivery including the use of a web-based programme. Cardiac Rehabilitation provides a structured, comprehensive programme, proven to reduce cardiovascular mortality and improve overall Quality of Life. However, as uptake remains relatively low with only 50% attending, exploring the benefits of offering a menu of programme options may allow greater patient choice and accessibility, meeting individual needs.

This study aims to compare how effective Cardiac Rehabilitation Programmes are on improving cardiovascular patients physical and mental wellbeing using a web-based compared with traditional cardiac rehab programmes in the hospital or through a combination of both.

Condition or Disease Intervention/Treatment Phase
  • Other: Hospital Based Cardiac Rehabilitation Exercise Classes
  • Other: Web-based Cardiac Rehabilitation Exercise Sessions
N/A

Detailed Description

This 8-week study, aims to compare quality of life (QOL), hospital anxiety and depression scores (HADs) and physical activity outcomes in web-based Cardiac Rehabilitation (CR), web-based CR combined with traditional CR (TCR) and TCR in patients with coronary heart disease (CHD).

The Web-based option will include the use of the MyHeart application.

Participants eligible for the study will include low-moderate cardiovascular patients (heart attack, stents or heart surgery) within 3-6 weeks post discharge. Participants will be involved in hospital or virtual exercise and educational sessions with the support of CR specialists. Primary outcomes will be measured through questionnaires and an incremental treadmill walking test.

To our knowledge, this would be the first study to compare all three groups, as combined CR (web-based alongside traditional CR) has not yet been evaluated. Additionally, the investigators currently work within the CR setting at Burton Hospital, and this study will be conducted within our current Hospital CR service. The outcomes will be applicable and relevant to future clinical practice.

As the UK's 50% uptake to CR remains poor, falling below the 85% national uptake recommendations, a CR menu-based approach, offering hospital or home-based programmes is recommended to encourage uptake, improve QOL and clinical outcomes.

Furthermore, as COVID-19 has enforced a web-based CR approach, further research to explore uptake, physical and psychological outcomes to benefit cardiovascular patients is paramount for current and future CR delivery.

This study will explore a menu of options recommended for CR.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
45 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Intervention Model Description:
Three way comparison study. Traditional Cardiac Rehabilitation Traditional Cardiac Rehabilitation combined with Web-based Cardiac Rehabilitation Web-based Cardiac RehabilitationThree way comparison study. Traditional Cardiac Rehabilitation Traditional Cardiac Rehabilitation combined with Web-based Cardiac Rehabilitation Web-based Cardiac Rehabilitation
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
To Examine the Effectiveness of Physical Activity, Quality of Life and Hospital Anxiety and Depression Outcomes in Cardiovascular Patients Using Either Traditional, Web-based or a Combined Cardiac Rehabilitation Programme.
Anticipated Study Start Date :
Jun 13, 2022
Anticipated Primary Completion Date :
Sep 13, 2022
Anticipated Study Completion Date :
Oct 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Traditional Cardiac Rehabilitation (Hospital based programme)

Traditional Cardiac Rehabilitation will involve 8 hospital-based exercise sessions, and one virtual education day over 8 weeks, supervised by CR health care professionals.

Other: Hospital Based Cardiac Rehabilitation Exercise Classes
Participants will attend 8 Hospital based CR exercise sessions. QOL and Hospital anxiety and Depression scores through questionnaires and incremental Shuttle Walk tests will be carried out pre and post intervention.

Experimental: Traditional combined with Web-based Cardiac Rehabilitation

Traditional combined with Web-based Cardiac Rehabilitation. Patients will attend 8 hospital-based exercise sessions and one virtual education day over 8-weeks with access to additional web-based (MyHeart app) exercise and educational information.

Other: Hospital Based Cardiac Rehabilitation Exercise Classes
Participants will attend 8 Hospital based CR exercise sessions. QOL and Hospital anxiety and Depression scores through questionnaires and incremental Shuttle Walk tests will be carried out pre and post intervention.

Other: Web-based Cardiac Rehabilitation Exercise Sessions
Participants will complete 8 weeks of Web-based CR exercise sessions using the MyHeart app. QOL and Hospital anxiety and Depression scores through questionnaires and incremental Shuttle Walk tests will be carried out pre and post intervention.

Experimental: Web-based Cardiac Rehabilitation

Web-based Cardiac Rehabilitation, using MyHeart app introduced during a pre-CR assessment, will follow an 8-week individualised self-managed platform, allowing contact with the CR health professionals via app messages only (no direct contact for web-based CR).

Other: Web-based Cardiac Rehabilitation Exercise Sessions
Participants will complete 8 weeks of Web-based CR exercise sessions using the MyHeart app. QOL and Hospital anxiety and Depression scores through questionnaires and incremental Shuttle Walk tests will be carried out pre and post intervention.

Outcome Measures

Primary Outcome Measures

  1. Energy Expenditure [The Walk Test will be completed pre and post intervention (8 weeks apart)]

    An Incremental Shuttle Walk test will be performed to determine the Metabolic equivalent achieved. Metabolic Equivalent (1 MET) is defined as the amount of energy required to serve the body's energy needs.

Secondary Outcome Measures

  1. Psychological outcome - Hospital Anxiety and Depression Score [Questionnaires will be given to the patient to complete pre and post intervention. (8 weeks apart)]

    This will be evaluated through participants completing a Hospital Anxiety and Depression questionnaire. Scoring range: 0-7 = normal range, 8-10 = borderline abnormal,11-21 abnormal and treatment is indicated.

  2. Psychological outcome - Dartmouth Coop Questionnaire [Questionnaires will be given to the patient to complete pre and post intervention. (8 weeks apart)]

    This will be evaluated through participants completing questions measuring health status, physical fitness, feelings, daily activities, social activities, change in health status, current overall health perceptions and bodily pain. Each question gives 5 response options, 1= very good, 2= good, 3= Moderate, 4=Bad, 5= Very Bad. Total score gives a profile of health status.

  3. Heart Rate [The Walk Test will be completed pre and post intervention (8 weeks apart)]

    An Incremental Shuttle Walk test will be performed to evaluate functional capacity and determine what percentage of predicted heart rate the participant has achieved. Heart Rate max will be calculated using the Karvonen Formula

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Low-moderate risk patients (low-mod Ejection Fraction (EF) (>40%), including clinically stable Myocardial Infarction (MI), Percutaneous Coronary Intervention (PCI), Coronary Artery Bypass Grafts (CABG) patients.

  • Acute patients, in-hospital patients (phase 3 rehab) to reflect true clinical representation.

  • Combination of male and female, as previous studies are predominately male.

  • Low-moderate Anxiety and depression scores (<11)

  • Achieve Level 4 (180metres, 5.1METs) on the Incremental Shuttle Walking Test

  • Internet and device access.

Exclusion Criteria:
  • <40% EF

  • High risk Heart Failure patients

  • Co-morbidities preventing exercise

  • No internet access

  • Unstable angina

  • Language barrier (English only, due to app)

  • Clinically depressed anxiety or depression scores (>11)

  • Incremental Shuttle Walk Test <Level 4 (180metres, 5.1METs)

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Derby and Burton NHS Foundation Trust Burton Upon Trent Staffordshire United Kingdom DE13 0RB

Sponsors and Collaborators

  • University of Chester
  • University Hospital of Derby and Burton NHS Foundation Trust

Investigators

  • Study Director: Mike Morris, University of Chester

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University of Chester
ClinicalTrials.gov Identifier:
NCT05326529
Other Study ID Numbers:
  • 290193
First Posted:
Apr 13, 2022
Last Update Posted:
May 23, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Chester
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 23, 2022