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Completed

NCT Number: NCT06178263

Adherence to an Exercise and Healthy Diet Program in Patients With Coronary Heart Disease Aged ≥ 60 Years

The purpose of the study is to implement a multimodal lifestyle intervention over 3 months in individuals ≥ 60 years of age with coronary heart disease and to examine the adherence to this intervention program. The intervention focus on three main themes: physical activity, healthy nutrition and, if necessary, smoking. The framework is formed by a psychological component: views on ageing.

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Key information

Age range

60 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Department of Preventive Resaerch and Social Medicine, Institute for Community Medicine, University Medicine Greifswald

Greifswald, 17489, Germany

About this study

Long-term adherence to a healthy lifestyle that promotes heart health (e.g. physical activity, healthy diet, non-smoking) is not yet sufficiently achieved in patients with coronary artery disease (≥ 60 years).

Individuals in this study will participate in a 3-month multimodal intervention program. The program includes group and individual sessions with a focus on exercise training and healthy nutrition. Positive views on ageing have been shown to be associated with a healthier lifestyle. Therefore, it seems important to consider views on ageing as part of a lifestyle intervention.

The intervention program starts with a group session containing information on (i) views on ageing and its association to lifestyle and (ii) how to cope with the diagnosis of coronary heart disease in everyday life.The physical exercise training and nutrition intervention will be carried out at least twice a week for at least 60 minutes each and for a period of 3 months. During this time, participants will receive instructions to exercise regularly and adjust their nutrition according to the recommendations. The physical exercise training and nutritional recommendations should be implemented at home. Study participants who smoke tobacco will be motivated to participate in a smoking cessation program. If they are not willing to do this, short, motivating interviews on smoking cessation will be offered.

A pilot study will be conducted using a pre-post design. Patients will be followed over time and data will be collected on anthropometrics, blood samples, cardiopulmonary exercise tests, and 7-day accelerometry at baseline and at 3- and 12-month follow-ups.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age of ≥ 60 years
  • established CVD defined by a stenosis of ≥ 70% of a least one coronary vessel
  • optimal treatment according to the European Society of Cardiology guidelines (2016)

Exclusion criteria

  • heart failure, left ventricular ejection fraction (LVEF) < 40%
  • implanted cardioverter/defibrillator or pacemaker
  • recent cardiovascular event ≤ 2 months prior to study inclusion (acute myocardial infarction, resuscitation, re-vascularization, device implantation, or stroke)
  • planned coronary revascularization
  • uncontrolled blood pressure (systolic blood pressure of ≥ 200 mmHg)
  • body mass index ≥ 35 kg/m2
  • baseline cardiopulmonary exercise test results precluding safe exercise training (e.g., ischemia or arrhythmias)
  • no ability to participate in exercise training (e.g., COPD GOLD III-IV, claudication ≥ 2b, or previous disabling stroke)
  • current mental disorder requiring inpatient treatment
  • current addictions (excluding tobacco use), florid psychoses, current severe depressive episode (according to ICD-10)
  • severe cognitive or physical impairment
  • no serious co-existing diseases (e.g., cancer) with life expectancy < 1 year
  • weekly self-reported PA ≥ 150 minutes on a moderate intensity level ≤ 6 months prior to study inclusion

Treatment and study plan

Primary outcomes

  1. Adherence to a multi-behavioral intervention program

    Time frame: Over 12 weeks (Baseline - 3-months)

    Investigation on (long-term) adherence to a 3-months multi-behavioral intervention program (exploratory); Measures: Documentation list of adherence to supervised physical exercise training program sessions, educational nutrition sessions, and views of ageing sessions.

  2. Feasibility of a multi-behavioral intervention program

    Time frame: Over 12 weeks (Baseline - 3-months)

    Investigation on the feasibility of the 3-months multi-behavioral intervention program (exploratory); Measures: Views of participants about study quality process (semi-structured interview guide including self-developed items; qualitative and quantitative)

Secondary outcomes

  1. Cardiopulmonary exercise testing

    Time frame: Changes from baseline (vs. 3-months and 12-months follow-up)

    Investigation on changes in a parameter of cardiopulmonary exercise testing (VO²max); Measures: standardized measurement of cardiopulmonary exercise testing according to a modified Jones protocol; VO²max in ml O²/min/kg

  2. Obesity marker

    Time frame: Changes from baseline (vs. 3-months and 12-months follow-up)

    Investigation on changes in an abdominal obesity marker (waist circumference); Measures: standardized measurements of waist circumference in cm

  3. Physical behavior by self-report

    Time frame: Changes from baseline (vs. 3-months and 12-months follow-up)

    Investigation on changes in physical behavior; Measures: assessement via questionnaire (Swiss Physical Activity Questionnaire, SWISSPAQ; DOI: https://doi.org/10.4414/smw.2013.13752); questionnaire includes 19 activities and 2 open answers for activities not listed. Patients had to specify the frequency (in times per week), duration (in minutes) and intensity (Borg's subjective rating of perceived exertion) of the activities that they performed in a typical week in the previous 2 months. Metric: MET-hours.

  4. Physical behavior by accelerometry (if valid data are available)

    Time frame: Changes from baseline (vs. 3-months and 12-months follow-up)

    Investigation on changes in physical behavior; Measures: objective measurement of physical behavior by 7-day accelerometry

  5. Smoking by self-report

    Time frame: Changes from baseline (vs. 3-months and 12-months follow-up)

    Investigation on changes in smoking; Measures: assessement via two self-reported items

  6. Cardiometabolic marker (I)

    Time frame: Changes from baseline (vs. 3-months and 12-months follow-up)

    Investigation on changes in plasma triglycerides (in mmol/l); Measures: standardized blood sampling

  7. Cardiometabolic marker (II)

    Time frame: Changes from baseline (vs. 3-months and 12-months follow-up)

    Investigation on changes in high-density lipoprotein cholesterol (in mmol/l); Measures: standardized blood sampling

  8. Cardiometabolic marker (III)

    Time frame: Changes from baseline (vs. 3-months and 12-months follow-up)

    Investigation on changes in glucose (in mmol/l); Measures: standardized blood sampling

  9. Brain-derived neurotrophic factor (BDNF)

    Time frame: Changes from baseline (vs. 3-months and 12-months follow-up)

    Investigation on changes in BDNF (in ng/ml); Measures: standardized blood sampling

  10. Blood pressure

    Time frame: Changes from baseline (vs. 3-months and 12-months follow-up)

    Investigation on changes in blood pressure; Measures: standardized measurements of mean blood pressure (in mmHg)

  11. Views on ageing

    Time frame: Changes from baseline (vs. 3-months and 12-months follow-up)

    Investigation on changes in views on ageing; Measures: assessement via questionnaire (Individual views on ageing: specific (physical loss, social loss, personal growth, gains) and global)

  12. Cardiac anxiety

    Time frame: Changes from baseline (vs. 3-months and 12-months follow-up)

    Investigation on changes in cardiac anxiety; Measures: assessement via questionnaire (Cardiac Anxiety Questionnaire, CAQ; DOI: 10.1016/s0005-7967(99)00132-1); 18-item, three subscales (Fear, 8 items; Avoidance, 5 items; Attention, 5 items). Each item is rated on a 5-point Likert scale with scores ranging from 0 (never) to 4 (always). A high score indicates a greater number of symptoms, greater frequency, or both.

  13. Nutrition

    Time frame: Changes from baseline (vs. 3-months and 12-months follow-up)

    Investigation on changes in nutrition; Measures: assessement via questionnaire (Mediterranean Diet Adherence Screener, MEDAS; doi: 10.1186/s12885-017-3337-y); 14 item, the MEDAS score can range between 0 and 14

Sponsors and collaborators

Lead sponsor

University Medicine Greifswald

Other

Collaborators

  • German Center of Cardiovascular Diseases (DZHK)

Registry information

Official study title

Adherence to an Exercise and Healthy Diet Program in Patients With Coronary

Acronym: RE-Start60+

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Dec 20, 2023
Registry last updated
Dec 20, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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