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Maintenance of Physical Activity After Cardiac Rehabilitation (FAIR)

Primary Purpose

Cardiovascular Diseases, Heart Diseases, Myocardial Ischemia

Status
Recruiting
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Maintenance intervention
Sponsored by
Slagelse Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cardiovascular Diseases focused on measuring cardiac rehabilitation, ischemic heart disease

Eligibility Criteria

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

Inclusion Criteria:

  • Age ≥18 years.
  • Participant in an exercise-based cardiac rehabilitation program in either hospital or municipality setting.
  • Access to a personal mobile phone and Danish telephone number.
  • Able to walk 3 meters without assistance.

Exclusion Criteria:

  • Insufficient Danish language proficiency to read and understand text messages and questionnaires.
  • Patients cognitively or mentally unable to participate.
  • Terminal patients and patients with a life expectancy of less than 3 months.

Sites / Locations

  • Holbæk HospitalRecruiting
  • City of Slagelse (municipality)Recruiting
  • Slagelse HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Maintenance intervention

Arm Description

Participants will receive a 12-week mobile health (mHealth) intervention that consists of action planning, text messages, and coordinator support.

Outcomes

Primary Outcome Measures

Recruitment
Green: Mean of ≥0.75 recruited participants per week per site Amber: Mean of 0.5-0.74 recruited participants per week per site Red: Mean of <0.5 recruited participants per week per site
Attrition/retention through follow-up assessment session
Green: ≥80% retention of participants through follow up Amber: 50-79% retention of participants through follow up Red: <50% retention of participants through follow up
Accelerometer data completeness
Green: Accelerometer data from both baseline and follow-up available on ≥80% of completing participants Amber: Data available on 50-79% of completing participants Red: Data available on <50% of completing participants
Accelerometer data completeness
Green: Accelerometer data from both baseline and follow-up available on ≥80% of completing participants Amber: Data available on 50-79% of completing participants Red: Data available on <50% of completing participants
Response rate on patient reported outcomes
Green: ≥90% of participants attending baseline and follow-up assessment return patient reported outcomes Amber: 75-89% of patients attending baseline and follow-up assessment return patient reported outcomes Red: <75% of participants attending baseline and follow-up assessment return patient reported outcomes
Response rate on patient reported outcomes
Green: ≥90% of participants attending baseline and follow-up assessment return patient reported outcomes Amber: 75-89% of patients attending baseline and follow-up assessment return patient reported outcomes Red: <75% of participants attending baseline and follow-up assessment return patient reported outcomes
Coordinator time spent, minutes per participant throughout the intervention
Green: Mean coordinator time spent of ≤30 minutes per participant Amber: Mean coordinator time spent of 31-60 minutes per participant Red: Mean coordinator time spent of >60 minutes per participant
Response rate (adherence) to weekly follow-up messages
Green: ≥75% of patients respond to at least 75% of messages Amber: 50-74% of patients respond to at least 75% of messages Red: <50% of patients respond to at least 75% of messages
Acceptability of text message component, single item
Green: ≥75% of participants find text messages acceptable Amber: 50-74% of participants find text messages acceptable Red: <50% of participants find text messages acceptable

Secondary Outcome Measures

Physical activity, objectively measured
Measured with thigh and wrist accelerometers
Physical function, walking
6 minute walking test
Physical function, sit-to-stand
30-second sit-to-stand test
Physical activity, subjectively measured
The International Physical Activity Questionnaire (IPAQ) is used to measure physical activity in the past 7 days. 0 is minimum (completely inactivty).

Full Information

First Posted
July 17, 2021
Last Updated
April 6, 2022
Sponsor
Slagelse Hospital
Collaborators
City of Slagelse (municipality), Holbaek Sygehus, University of Southern Denmark, University College Copenhagen
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1. Study Identification

Unique Protocol Identification Number
NCT05011994
Brief Title
Maintenance of Physical Activity After Cardiac Rehabilitation
Acronym
FAIR
Official Title
Maintenance of Physical Activity After Cardiac Rehabilitation: a Feasibility Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Recruiting
Study Start Date
August 30, 2021 (Actual)
Primary Completion Date
April 30, 2022 (Anticipated)
Study Completion Date
April 30, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Slagelse Hospital
Collaborators
City of Slagelse (municipality), Holbaek Sygehus, University of Southern Denmark, University College Copenhagen

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Physical activity is a key element in cardiac rehabilitation and prevention of cardiovascular mortality and hospitalizations. After cardiac rehabilitation programs end, physical activity levels and participation in continued cardiac rehabilitation declines. The aim of this study is to evaluate the feasibility a mobile health intervention with text messages and behavior change theory in patients with cardiovascular disease for a duration of 3 months after completion of a cardiac rehabilitation program. An intervention consisting of action planning, text messages, and coordinator support is tested in a feasibility trial design with 40 expected participants.
Detailed Description
Physical activity is a key element in cardiac rehabilitation and prevention of cardiovascular mortality and hospitalizations. After cardiac rehabilitation programs end, physical activity levels and participation in continued cardiac rehabilitation declines. The primary aim of this study is to evaluate the feasibility in terms of recruitment, retention, data completeness, intervention delivery and compliance, and acceptability of a mobile health intervention with text messages and behavior change theory in patients with cardiovascular disease for a duration of 3 months after completion of a cardiac rehabilitation program. The study is a single-group multi-site feasibility trial. Participants will be recruited from phase II cardiac rehabilitation programs at Slagelse Hospital, the city of Slagelse (municipality), and Holbæk Hospital. Starting immediately after completion of cardiac rehabilitation, study participants will receive an intervention that consists of action planning, text messages, and coordinator support for a period of 12 weeks (see more details under 'Arms and Interventions'). The investigators base the intervention on a theoretical model of behavior change in the form of the Health Action Process Approach (HAPA). Behavior change techniques (BCTs) are used as part of the intervention. The intervention is an addition to standard practice and does not replace any existing treatment offers. To evaluate the feasibility of the intervention and its readiness to be tested in a subsequent RCT design, the investigators have set progression criteria using a system of green (proceed to RCT), amber (amend when proceeding to RCT), or red (issue must be solved before proceeding to RCT). The progression criteria are listed under 'Primary Outcome Measures'. Participants will wear accelerometers on thigh and wrist for 1 and 3 weeks, respectively, starting 1 week before end of cardiac rehabilitation. Baseline measurements and start of intervention is planned to be at the same time as cardiac rehabilitation ends. After 11 weeks of intervention, participants will attend a follow-up assessment, where participants will wear accelerometers on thigh and wrist again.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiovascular Diseases, Heart Diseases, Myocardial Ischemia, Heart Failure, Arrythmia, Heart Arrest
Keywords
cardiac rehabilitation, ischemic heart disease

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Maintenance intervention
Arm Type
Experimental
Arm Description
Participants will receive a 12-week mobile health (mHealth) intervention that consists of action planning, text messages, and coordinator support.
Intervention Type
Behavioral
Intervention Name(s)
Maintenance intervention
Intervention Description
The intervention consists of action planning, text messages, and coordinator support. At onset, each participant creates an action plan for physical activity with the help of a health professional: What types of physical activities? When and how often? Where and with who? 2 auto-generated text messages are sent weekly for a duration of 12 weeks. The first prompts physical activity. The second asks if plans were reached. If yes, an automatic reply with positive reinforcement is generated. If no, an automatic reply asks if the participant wants to be contacted. Participants are contacted by a coordinator either by answering text messages or if not answering the texts for a period of 2 weeks or more. Coordinator functions: Call participants replying to texts that they wish to be contacted Help participants establish contact to local activities involving physical activity Follow-up on and adjustment of action plan Offer guidance in physical activity
Primary Outcome Measure Information:
Title
Recruitment
Description
Green: Mean of ≥0.75 recruited participants per week per site Amber: Mean of 0.5-0.74 recruited participants per week per site Red: Mean of <0.5 recruited participants per week per site
Time Frame
Baseline
Title
Attrition/retention through follow-up assessment session
Description
Green: ≥80% retention of participants through follow up Amber: 50-79% retention of participants through follow up Red: <50% retention of participants through follow up
Time Frame
Up to 12 weeks
Title
Accelerometer data completeness
Description
Green: Accelerometer data from both baseline and follow-up available on ≥80% of completing participants Amber: Data available on 50-79% of completing participants Red: Data available on <50% of completing participants
Time Frame
Baseline
Title
Accelerometer data completeness
Description
Green: Accelerometer data from both baseline and follow-up available on ≥80% of completing participants Amber: Data available on 50-79% of completing participants Red: Data available on <50% of completing participants
Time Frame
12 weeks
Title
Response rate on patient reported outcomes
Description
Green: ≥90% of participants attending baseline and follow-up assessment return patient reported outcomes Amber: 75-89% of patients attending baseline and follow-up assessment return patient reported outcomes Red: <75% of participants attending baseline and follow-up assessment return patient reported outcomes
Time Frame
Baseline
Title
Response rate on patient reported outcomes
Description
Green: ≥90% of participants attending baseline and follow-up assessment return patient reported outcomes Amber: 75-89% of patients attending baseline and follow-up assessment return patient reported outcomes Red: <75% of participants attending baseline and follow-up assessment return patient reported outcomes
Time Frame
12 weeks
Title
Coordinator time spent, minutes per participant throughout the intervention
Description
Green: Mean coordinator time spent of ≤30 minutes per participant Amber: Mean coordinator time spent of 31-60 minutes per participant Red: Mean coordinator time spent of >60 minutes per participant
Time Frame
12 weeks
Title
Response rate (adherence) to weekly follow-up messages
Description
Green: ≥75% of patients respond to at least 75% of messages Amber: 50-74% of patients respond to at least 75% of messages Red: <50% of patients respond to at least 75% of messages
Time Frame
12 weeks
Title
Acceptability of text message component, single item
Description
Green: ≥75% of participants find text messages acceptable Amber: 50-74% of participants find text messages acceptable Red: <50% of participants find text messages acceptable
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Physical activity, objectively measured
Description
Measured with thigh and wrist accelerometers
Time Frame
Change from baseline to 12 weeks
Title
Physical function, walking
Description
6 minute walking test
Time Frame
Change from baseline to 12 weeks
Title
Physical function, sit-to-stand
Description
30-second sit-to-stand test
Time Frame
Change from baseline to 12 weeks
Title
Physical activity, subjectively measured
Description
The International Physical Activity Questionnaire (IPAQ) is used to measure physical activity in the past 7 days. 0 is minimum (completely inactivty).
Time Frame
Change from baseline to 12 weeks
Other Pre-specified Outcome Measures:
Title
Health-related quality of life, general
Description
EQ-5D-5L evaluates health status in 5 dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension is rated from 1 (best) to 5 (worst) and overall health is rated on a 0 to 100 VAS scale.
Time Frame
Change from baseline to 12 weeks
Title
Health-related quality of life, VAS subscale
Description
EQ-5D-5L evaluates health status in 5 dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension is rated from 1 (best) to 5 (worst) and overall health is rated on a 0 to 100 VAS scale.
Time Frame
Change from baseline to 12 weeks
Title
Health-related quality of life, heart-specific
Description
HeartQoL is used to measure heart-specific quality of life in the past 4 weeks. Range from 0 (worst) to 42 (best) .
Time Frame
Change from baseline to 12 weeks
Title
Anxiety and depression
Description
Hospital Anxiety and Depression Scale (HADS). HADS gives a score for each of anxiety and depression, each ranging from 0 (best) to 21 (worst).
Time Frame
Change from baseline to 12 weeks
Title
Physical function, self-reported
Description
WHO Disability Assessment Schedule 2.0 (WHODAS 2.0),12-item version. WHODAS is a generic assessment instrument for health and disability. Range from 12 (no disability) to 60 (highest disability or loss of function).
Time Frame
Change from baseline to 12 weeks
Title
Comorbidity
Description
Disease Burden: Morbidity Assessment by Self-Report used to evaluated a list of common chronic conditions affect the participants' daily activities. Each condition (that the participant has) is rated from 1 (not at all) to 5 (a lot) in regard to how much it limits daily activities.
Time Frame
Change from baseline to 12 weeks
Title
Self-efficacy, managing chronic disease
Description
Self-efficacy of managing chronic disease 6 items scale. Score is calculated as the mean of 6 items, each scored from 1 (low self-efficacy) to 10 (high self-efficacy).
Time Frame
Change from baseline to 12 weeks
Title
Motivational Self-efficacy
Description
Motivational self-efficacy, HAPA items by Schwartzer R., 2 items each rated on a scale from 1 (low self-efficacy) to 4 (high self-efficacy).
Time Frame
Change from baseline to 12 weeks
Title
Coping Self-efficacy
Description
Coping self-efficacy, HAPA items by Schwartzer R., 2 items each rated on a scale from 1 (low self-efficacy) to 4 (high self-efficacy).
Time Frame
Change from baseline to 12 weeks
Title
Recovery Self-efficacy
Description
Recovery self-efficacy, HAPA items by Schwartzer R., 2 items each rated on a scale from 1 (low self-efficacy) to 4 (high self-efficacy).
Time Frame
Change from baseline to 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥18 years. Participant in an exercise-based cardiac rehabilitation program in either hospital or municipality setting. Access to a personal mobile phone and Danish telephone number. Able to walk 3 meters without assistance. Exclusion Criteria: Insufficient Danish language proficiency to read and understand text messages and questionnaires. Patients cognitively or mentally unable to participate. Terminal patients and patients with a life expectancy of less than 3 months.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rune M Andersen, PhD
Phone
+4529623522
Ext
+4558559790
Email
ruma@regionsjaelland.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Lars H Tang, PhD
Phone
+4558559790
Email
larta@regionsjaelland.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rune M Andersen, PhD
Organizational Affiliation
Næstved-Slagelse-Ringsted Hospitals; University of Southern Denmark
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Lars H Tang, PhD
Organizational Affiliation
Næstved-Slagelse-Ringsted Hospitals; University of Southern Denmark
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Søren T Skou, PhD
Organizational Affiliation
Næstved-Slagelse-Ringsted Hospitals; University of Southern Denmark
Official's Role
Study Chair
Facility Information:
Facility Name
Holbæk Hospital
City
Holbæk
ZIP/Postal Code
4300
Country
Denmark
Individual Site Status
Recruiting
Facility Name
City of Slagelse (municipality)
City
Korsør
ZIP/Postal Code
4220
Country
Denmark
Individual Site Status
Recruiting
Facility Name
Slagelse Hospital
City
Slagelse
ZIP/Postal Code
4200
Country
Denmark
Individual Site Status
Recruiting

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35383088
Citation
Andersen RM, Skou ST, Clausen MB, Jager M, Zangger G, Grontved A, Brond JC, Soja AMB, Tang LH. Maintenance of physical activity after cardiac rehabilitation (FAIR): study protocol for a feasibility trial. BMJ Open. 2022 Apr 5;12(4):e060157. doi: 10.1136/bmjopen-2021-060157.
Results Reference
derived
Links:
URL
https://bmjopen.bmj.com/content/12/4/e060157.info
Description
Link to published study protocol

Learn more about this trial

Maintenance of Physical Activity After Cardiac Rehabilitation

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