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A Trial of a Home Based Walking Program as an Alternate Program for Non Attenders at Cardiac Rehabilitation (CRU-SHAL)

Primary Purpose

Acute Myocardial Infarction

Status
Withdrawn
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
home-based walking program
Sponsored by
Queen's University, Belfast
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Acute Myocardial Infarction focused on measuring Cardiac Rehabilitation, Walking, Acute Myocardial Infarction, Secondary Prevention

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Justification of diagnosis of myocardial infarction by report of cardiac bio-markers or electrocardiogram changes Exclusion Criteria - planned for RCT - applied to small pilot: Heart failure/ Cardiogenic shock Complex ventricular arrhythmias Mental/physical impairment (exclude if housebound/dementia) Valve disorder-severe stenotic or regurgitant lesion Hypertrophic cardiomyopathy Exercise Stress Test result- exclude if ST depression>=2 mm or angina at <5 Metabolic Equivalent of Tasks (METS) (e.g. 3 minutes of a Bruce protocol). (Also exclude if report of ST segment depression >=1 mm on resting ECG )

Sites / Locations

  • Dept of General Practice

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

1 - home-based walking program

2 - cardiac rehabilitation

Arm Description

Based on medical record held in general practice, patients who had not attended a formal cardiac rehabilitation program after myocardial infarction and were enrolled in home-based walking programme

Based on medical record held in general practice, patients who are identified as having attended a Cardiac Rehabilitation program following myocardial infarction - 'usual care'

Outcomes

Primary Outcome Measures

Quality of Life Score
MacNew Post-myocardial infarction questionnaire score

Secondary Outcome Measures

Full Information

First Posted
September 19, 2005
Last Updated
February 4, 2022
Sponsor
Queen's University, Belfast
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1. Study Identification

Unique Protocol Identification Number
NCT00219830
Brief Title
A Trial of a Home Based Walking Program as an Alternate Program for Non Attenders at Cardiac Rehabilitation
Acronym
CRU-SHAL
Official Title
Health and Social Inequalities in the Uptake of Cardiac Rehabilitation in Northern Ireland: an Alternative Program for Non-attenders: (2) a Randomised Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Withdrawn
Why Stopped
no invited participants agreed to undertake the proposed intervention
Study Start Date
January 2005 (Anticipated)
Primary Completion Date
May 2007 (Anticipated)
Study Completion Date
May 2007 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Queen's University, Belfast

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to investigate if a home-based walking program is an acceptable alternative for those who choose not to attend formal cardiac rehabilitation programs and if such a program has an effect on coronary risk or physical fitness.
Detailed Description
Coronary heart disease (CHD) is the most important cause of life years lost in Northern Ireland (NI). A recently updated Cochrane review (Joliffe et al, 2003) confirmed the findings of earlier meta-analyses (O'Connor et al, 1989; Oldridge et al, 1988) which indicated that participation in cardiac rehabilitation (CR) reduces mortality after MI. The earlier work demonstrated a reduction of 20-25% in all-cause and cardiac mortality. The recent work allowed analysis of an increased number of patients (8440 in 32 trials) and reported a reduction in total cardiac mortality of up to 31%. Participation in CR after MI also improves well-being and reduces disability (NHS, 1998). However, informal reports suggest that only approximately 50% of patients actually attend a hospital based program. The hypothesis to be tested is that for those who chose not to attend formal CR, a home-based walking program is an acceptable alternative. This programme of work entails two separate study designs. To evaluate the home-based walking program, we plan a randomised controlled trial (RCT). Randomisation of subjects to study groups will follow determination of eligibility to participate. Participants randomised to the experimental group will be asked to walk for up to 30 minutes, 5-days per week. They will be requested to record aspects of their walking in a diary, including time, intensity and number of steps taken (recorded using a pedometer). Qualitative methodology using semi-structured interviews will be used to explore the experiences of those allocated to the intervention group. The attitudes and experiences of other non-attenders of CR who declined to participate in the trial will be explored in focus groups. Three focus groups each containing 8 participants are planned. Focus group transcripts will be analysed independently by two observers using a computer program (NUDIST) to identify themes and develop questions for the semi-structured interviews. Analysis of the semi-structured interviews will be descriptive, responses being categorised into themes as appropriate. RCT results will be analysed by intention to treat.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Myocardial Infarction
Keywords
Cardiac Rehabilitation, Walking, Acute Myocardial Infarction, Secondary Prevention

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1 - home-based walking program
Arm Type
Experimental
Arm Description
Based on medical record held in general practice, patients who had not attended a formal cardiac rehabilitation program after myocardial infarction and were enrolled in home-based walking programme
Arm Title
2 - cardiac rehabilitation
Arm Type
No Intervention
Arm Description
Based on medical record held in general practice, patients who are identified as having attended a Cardiac Rehabilitation program following myocardial infarction - 'usual care'
Intervention Type
Behavioral
Intervention Name(s)
home-based walking program
Intervention Description
Home-based walking program; included use of pedometer and daily walk diary
Primary Outcome Measure Information:
Title
Quality of Life Score
Description
MacNew Post-myocardial infarction questionnaire score
Time Frame
16-20 weeks post myocardial infarction

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Justification of diagnosis of myocardial infarction by report of cardiac bio-markers or electrocardiogram changes Exclusion Criteria - planned for RCT - applied to small pilot: Heart failure/ Cardiogenic shock Complex ventricular arrhythmias Mental/physical impairment (exclude if housebound/dementia) Valve disorder-severe stenotic or regurgitant lesion Hypertrophic cardiomyopathy Exercise Stress Test result- exclude if ST depression>=2 mm or angina at <5 Metabolic Equivalent of Tasks (METS) (e.g. 3 minutes of a Bruce protocol). (Also exclude if report of ST segment depression >=1 mm on resting ECG )
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Margaret E Cupples, MD
Organizational Affiliation
Queen's University, Belfast
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mark A Tully, PhD
Organizational Affiliation
Queen's University, Belfast
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dept of General Practice
City
Belfast
State/Province
Northern Ireland
ZIP/Postal Code
BT9 7HR
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
No plan to share individual participant data - these will form an aggregated database for determination of the design of a later definitive study.
Citations:
Citation
Tully M, Cupples ME, Young IS et al. CRU-SHAL Study - provision and uptake of cardiac rehabilitation in Northern Ireland. British Association for Cardiac Rehabilitation Annual Conference: Emerging Challenges for Cardiac Rehabilitation. September 2006, p10.
Results Reference
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A Trial of a Home Based Walking Program as an Alternate Program for Non Attenders at Cardiac Rehabilitation

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