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Behavioral Interventions for Improvement of Adherence at Exercise-based Cardiac Rehabilitation (ECRA) (ECRA)

Primary Purpose

Coronary Artery Disease

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Extended behavioral intervention
Sponsored by
Linkoeping University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Disease focused on measuring Exercise-based cardiac rehabilitation, Physical capacity, Adherence, Behavioral medicine

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Primary care event due to coronary artery disease and/or percutaneous coronary intervention (PCI) at the coronary care unit, Linköping University hospital
  • Age <75 years

Exclusion Criteria:

  • Serious physical or psychological disease interfering with participation in exercise-based CR
  • Inability to understand the Swedish language

Sites / Locations

  • Linkoeping University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Extended behavioral intervention

Usual care

Arm Description

Specific goal-setting, self-monitoring and feed-back

Hospital-based or home-based aerobic exercise 3 times a week with a duration of 30-60 minutes and an intensity of 40-80 % of Vo2max and resistance exercise 2 times a week of 1-3 sets of 10-15 repetitions. The exercise period is 16 weeks.

Outcomes

Primary Outcome Measures

Change from baseline aerobic exercise capacity (watts) at 4 months
The test is performed on a bicycle ergometer according to the WHO-protocol with an increased workload of 25W every 4.5 minutes.The exercise test is discontinued at Borg RPE 17 and/or dyspnea 7 at Borg´s CR-10 scale.

Secondary Outcome Measures

Adherence to dose of exercise
accelerometer
Adherence to dose in exercise
exercise diary
Change from baseline unilateral isotonic shoulder flexion (repetitions) at 4 months
Muscle endurance test
Change from baseline unilateral isotonic heel lift (repetitions) at 4 months
Muscle endurance test
Change from baseline anxiety score at 4 months
Hospital Anxiety and Depression Scale (HADS)
Change from baseline depression score at 4 months
Hospital Anxiety and Depression Scale (HADS)
Change from baseline self-efficacy score at 4 months
Self Efficacy Exercise Scale (SEE-SV)
Change from baseline health-related quality of life score at 4 months
Short-Form-36 (SF-36)
Change from baseline health-related quality of life score at 4 months
EQ5D
Change from baseline level of physical activity at 4 months
Accelerometer
Change from baseline level of physical activity at 4 months
Bouchard questionnaire
Change from baseline aerobic exercise capacity (watts) at 12 months
Submaximal exercise test on bicycle ergometer
Adherence to dose of exercise
Accelerometer
Adherence to dose of exercise
Exercise diary
Change from baseline unilateral isotonic shoulder flexion (repetitions) at 12 months
Muscle endurance test
Change from baseline unilateral isotonic heel lift (repetitions) at 12 months
Muscle endurance test
Change from baseline anxiety score at 12 months
Hospital Anxiety and Depression Scale (HADS)
Change from baseline depression score at 12 months
Hospital Anxiety and Depression Scale (HADS)
Change from baseline self-efficacy score at 12 months
Self Efficacy Exercise Scale (SEE-SV)
Change from baseline health-related quality of life score at 12 months
Short-Form-36 (SF-36)
Change from baseline health-related quality of life score at 12 months
EQ5D
Change from baseline level of physical activity at 12 months
accelerometer
Change from baseline level of physical activity at 12 months
Bouchard questionnaire
Patient Enablement (score)
Patient Enablement Instrument (PEI)

Full Information

First Posted
August 16, 2016
Last Updated
October 15, 2021
Sponsor
Linkoeping University
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1. Study Identification

Unique Protocol Identification Number
NCT02895451
Brief Title
Behavioral Interventions for Improvement of Adherence at Exercise-based Cardiac Rehabilitation (ECRA)
Acronym
ECRA
Official Title
Behavioral Interventions for Improvement of Adherence at Exercise-based Cardiac Rehabilitation (ECRA)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
December 15, 2016 (undefined)
Primary Completion Date
April 15, 2019 (Actual)
Study Completion Date
June 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Linkoeping University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to investigate the effects of an extended behavioral intervention in exercise-based CR for improvement of physical capacity, adherence, psychological and physiological parameters, compared with usual care.
Detailed Description
Consecutive patients will be included at the coronary care unit (CCU), Linköping University Hospital, Sweden. Physiotherapists ask patients for informed consent at the CCU and book an appointment at the exercise-based CR 2-3 weeks after discharge for baseline tests. After baseline testing patients will be randomized to either extended intervention or routine care. Randomization will be stratified by submaximal exercise capacity. Patients randomized to the extended intervention group receive an additional appointment to a physiotherapist within a week. Thereafter patients in both groups start the exercise-based CR program, including aerobic exercise and resistance exercise, 3 times/week for 16 weeks, according to international guidelines for exercise-based CR. The extended intervention is based on components from behavioral medicine including: specific goal-setting, self-monitoring and feed-back. Changes in the endpoint variables will be measured from baseline to first (16 weeks at end of intervention) and second (12 months after index event) follow-up visits. Sample size calculations are based on previous clinical data from a similar exercise-based CR setting (n=50) on differences in aerobic exercise capacity measured by submaximal exercise test (watts) before vs after finished exercise-based CR. With a power of 80% and a two-sided significance level of p<0.05 and least mean difference at 10 watts (SD 20 watts) and a calculated loss of follow-up of 20%, the estimated sample size is 160 patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease
Keywords
Exercise-based cardiac rehabilitation, Physical capacity, Adherence, Behavioral medicine

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
170 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Extended behavioral intervention
Arm Type
Experimental
Arm Description
Specific goal-setting, self-monitoring and feed-back
Arm Title
Usual care
Arm Type
No Intervention
Arm Description
Hospital-based or home-based aerobic exercise 3 times a week with a duration of 30-60 minutes and an intensity of 40-80 % of Vo2max and resistance exercise 2 times a week of 1-3 sets of 10-15 repetitions. The exercise period is 16 weeks.
Intervention Type
Behavioral
Intervention Name(s)
Extended behavioral intervention
Intervention Description
The exercise goal is set in liaison between the patient and the physiotherapist, based on activities and target behaviors that the patient thinks is relevant and important. The patients are asked to self-monitor the defined exercise goal by completing an exercise diary. The exercise diary includes specification of the performed exercise dose (frequency, intensity and duration). The exercise diary is followed up by a physiotherapist every third week by a phone call or a personal meeting. Visual feed-back on the performed dose of exercise is given once by accelerometry. At end of intervention (16 weeks) the patient is offered a follow-up meeting with the physiotherapist to discuss a long-term exercise goal.
Primary Outcome Measure Information:
Title
Change from baseline aerobic exercise capacity (watts) at 4 months
Description
The test is performed on a bicycle ergometer according to the WHO-protocol with an increased workload of 25W every 4.5 minutes.The exercise test is discontinued at Borg RPE 17 and/or dyspnea 7 at Borg´s CR-10 scale.
Time Frame
4 months
Secondary Outcome Measure Information:
Title
Adherence to dose of exercise
Description
accelerometer
Time Frame
4 months
Title
Adherence to dose in exercise
Description
exercise diary
Time Frame
4 months
Title
Change from baseline unilateral isotonic shoulder flexion (repetitions) at 4 months
Description
Muscle endurance test
Time Frame
4 months
Title
Change from baseline unilateral isotonic heel lift (repetitions) at 4 months
Description
Muscle endurance test
Time Frame
4 months
Title
Change from baseline anxiety score at 4 months
Description
Hospital Anxiety and Depression Scale (HADS)
Time Frame
4 months
Title
Change from baseline depression score at 4 months
Description
Hospital Anxiety and Depression Scale (HADS)
Time Frame
4 months
Title
Change from baseline self-efficacy score at 4 months
Description
Self Efficacy Exercise Scale (SEE-SV)
Time Frame
4 months
Title
Change from baseline health-related quality of life score at 4 months
Description
Short-Form-36 (SF-36)
Time Frame
4 months
Title
Change from baseline health-related quality of life score at 4 months
Description
EQ5D
Time Frame
4 months
Title
Change from baseline level of physical activity at 4 months
Description
Accelerometer
Time Frame
4 months
Title
Change from baseline level of physical activity at 4 months
Description
Bouchard questionnaire
Time Frame
4 months
Title
Change from baseline aerobic exercise capacity (watts) at 12 months
Description
Submaximal exercise test on bicycle ergometer
Time Frame
12 months
Title
Adherence to dose of exercise
Description
Accelerometer
Time Frame
12 months
Title
Adherence to dose of exercise
Description
Exercise diary
Time Frame
12 months
Title
Change from baseline unilateral isotonic shoulder flexion (repetitions) at 12 months
Description
Muscle endurance test
Time Frame
12 months
Title
Change from baseline unilateral isotonic heel lift (repetitions) at 12 months
Description
Muscle endurance test
Time Frame
12 months
Title
Change from baseline anxiety score at 12 months
Description
Hospital Anxiety and Depression Scale (HADS)
Time Frame
12 months
Title
Change from baseline depression score at 12 months
Description
Hospital Anxiety and Depression Scale (HADS)
Time Frame
12 months
Title
Change from baseline self-efficacy score at 12 months
Description
Self Efficacy Exercise Scale (SEE-SV)
Time Frame
12 months
Title
Change from baseline health-related quality of life score at 12 months
Description
Short-Form-36 (SF-36)
Time Frame
12 months
Title
Change from baseline health-related quality of life score at 12 months
Description
EQ5D
Time Frame
2 months
Title
Change from baseline level of physical activity at 12 months
Description
accelerometer
Time Frame
12 months
Title
Change from baseline level of physical activity at 12 months
Description
Bouchard questionnaire
Time Frame
12 months
Title
Patient Enablement (score)
Description
Patient Enablement Instrument (PEI)
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Primary care event due to coronary artery disease and/or percutaneous coronary intervention (PCI) at the coronary care unit, Linköping University hospital Age <75 years Exclusion Criteria: Serious physical or psychological disease interfering with participation in exercise-based CR Inability to understand the Swedish language
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maria Bäck, PhD
Organizational Affiliation
Linkoeping University, Department of Medical and Health Sciences, Division of Physiotherapy
Official's Role
Study Chair
Facility Information:
Facility Name
Linkoeping University
City
Linkoeping
ZIP/Postal Code
58183
Country
Sweden

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32419950
Citation
Freene N, Borg S, McManus M, Mair T, Tan R, Davey R, Oberg B, Back M. Comparison of device-based physical activity and sedentary behaviour following percutaneous coronary intervention in a cohort from Sweden and Australia: a harmonised, exploratory study. BMC Sports Sci Med Rehabil. 2020 May 9;12:17. doi: 10.1186/s13102-020-00164-1. eCollection 2020.
Results Reference
derived
PubMed Identifier
28545400
Citation
Borg S, Oberg B, Nilsson L, Soderlund A, Back M. The role of a behavioural medicine intervention in physiotherapy for the effects of rehabilitation outcomes in exercise-based cardiac rehabilitation (ECRA) - the study protocol of a randomised, controlled trial. BMC Cardiovasc Disord. 2017 May 25;17(1):134. doi: 10.1186/s12872-017-0557-7.
Results Reference
derived

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Behavioral Interventions for Improvement of Adherence at Exercise-based Cardiac Rehabilitation (ECRA)

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