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NCT Number: NCT06646601

A Preventive, Multidisciplinary Primary Care Intervention Organized Around a Therapeutic Garden: Acceptability to Patients Suffering from Cardio-neurovascular Pathology and to Those Involved in the Action.

A preventive, multidisciplinary primary care intervention organized around a therapeutic garden: Acceptability to patients suffering from cardio-neurovascular pathology and to those involved in the action.

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Key information

Conditions

Vascular Disease Arrhythmias, Cardiac Atrial Fibrillation Atrial Fibrillation (AF) Brain Diseases Cardiomyopathies Cardiovascular Cardiovascular Diseases Central Nervous System Diseases Cerebrovascular Disorders Heart Diseases Heart Failure NYHA Class II Hypertension Resistant to Conventional Therapy Ischemic Stroke Nervous System Diseases Pathologic Processes Pathological Conditions, Signs and Symptoms Stroke Stroke, Ischemic Vascular Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • age > 18 years old;
  • living in the vicinity (+-20 km) of Gap, Laragne-Montéglin, Veynes and Clermont-Ferrand;
  • having been invited to take part in the intervention by the caregivers of the medical structures
  • suffering from an ALD based on CNAM medical criteria (stroke, AOMI, rhythm disorders, valvular heart disease, congenital heart disease, stage I and II heart failure), severe hypertension, chronic coronary disease)

Exclusion criteria

  • heart failure based on CNAM medical criteria (ALD n°5) stage III and IV according to NYHA classification ;
  • with a contraindication to physical activity ;
  • living in an institution;
  • unable to walk more than 100 m independently;
  • Alzheimer's disease or other dementias based on CNAM medical criteria ;
  • with an unlabelled cognitive impairment limiting comprehension.

Treatment and study plan

Intervention of prevention

Other

A 6-month multidisciplinary preventive intervention for each patient: gardening, adapted physical activity, nutritional workshops.

Primary outcomes

  1. Acceptance rate of intervention

    Time frame: From enrollment to the end of treatment at 6 months

    Assessing the acceptability of a multidisciplinary intervention combining gardening activities, APA and nutrition workshops, organized around a therapeutic garden, by patients suffering from cardio-neurovascular pathologies and the interveners of the action.

  2. Identification of the obstacles and facilitators for intervention

    Time frame: From enrollment to the end of treatment at 6 months

    Identify the obstacles and factors facilitating patients' initial adhesion to and commitment to the scheme, and those influencing the implementation of the action by those involved, i.e. the facilitators and caregivers involved.

Secondary outcomes

  1. Assessing the impact of the intervention

    Time frame: From enrollment to the end of treatment at 6 months

    Assess the impact of the intervention on quality of life, adoption of new lifestyle habits (PA and Mediterranean diet), depressive symptoms and physical performance, taking into account any adverse effects.

Study contacts

Contact information is provided by the study sponsor or research team.

Julie Gardette, Dr

CONTACT

[email protected]

+33491381245

Sponsors and collaborators

Lead sponsor

Assistance Publique Hopitaux De Marseille

Other

Registry information

Acronym: ArTERRE

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Oct 17, 2024
Registry last updated
Oct 17, 2024

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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