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Completed

NCT Number: NCT06815484

Preventing Burnout Among Caregivers Through Physical Activity

The purpose of this study is to evaluate the impact of an adaptive physical activity programme to prevent the risk of burnout at the end of the programme (10 weeks after the start of the intervention).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Clinique de la Sauvegarde

Lyon, 69009, France

About this study

The PACA trial is a pilot, prospective, comparative, randomised (2 arms), controlled, single-centre study.

The study population consisted of adult healthcare professionals at the Clinique de la Sauvegarde with a low to moderate level of physical activity and no contraindications to physical activity.

Participants will be randomised into two arms (ratio 1:1):

  • Arm A (intervention): Participants will benefit from an adaptive physical activity programme supervised by a physical activity professional over a 9-week period.
  • Arm B (control): Participants will receive the recommendations of the world health organisation for physical activity.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Age > 18 years ;
  • Non-physician health professionals at the Clinique de la Sauvegarde ;
  • Low or moderate level of physical activity, as assessed by the questionnaire International Physical Activity Questionnaire. In fact, work-related physical activity is not associated with a reduction in burnout ;
  • Absence of serious chronic pathology incompatible with the physical activity of the protocol ;
  • Willing and available to commit to the project for the duration of the study ;
  • Using a personal smartphone or tablet and with an Internet connection ;
  • Able to read, write and understand French ;
  • Membership of a social security scheme.

Exclusion criteria

  • High level of physical activity (not including work-related physical activity) ;
  • Contraindication to physical activity (uncontrolled hypertension, uncontrolled heart disease...) ;
  • Concurrent participation in another physical activity study ;
  • Pregnant or likely to be pregnant ;
  • Unable to be monitored for medical, social, family, geographical or psychological reasons for the duration of the study ;
  • Persons deprived of their liberty by judicial or adm inistrative decision, or adults protected by law.

Treatment and study plan

Intervention group with physical activity programme

Other

Programme comprising active breaks to be incorporated into daily life, supervised group physical activity sessions with personalised advice and a motivational interview with a physical activity professional to encourage regular physical activity.

Recommendations of the World Health Organisation

Other

The World Health Organisation's recommendations on physical activity, which recommend at least 150 minutes a week of moderate-intensity activity or 75 minutes of high-intensity activity, and highlight the importance of limiting sedentary behaviour.

Primary outcomes

  1. Shirom - Melamed Burnout Measure

    Time frame: 10 weeks

    The primary endpoint is the burnout will be measured by the score on the Shirom - Melamed Burnout Measure questionnaire.

    The validated French version of the Shirom-Melamed Burnout Measure comprises 14 items assessed on a Likert scale from 1 (never) to 7 (always), quantifying the frequency of symptoms experienced over the last seven days.

Sponsors and collaborators

Lead sponsor

GCS Ramsay Santé pour l'Enseignement et la Recherche

Other

Collaborators

  • Euraxi Pharma

Registry information

Official study title

Single-centre, Randomised, Controlled Study Designed to Evaluate the Impact of a Nine-week Supervised Physical Activity Programme Physical Activity Programme on Reducing the Risk of Burnout in Burnout in Carers

Acronym: PACA

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Feb 7, 2025
Registry last updated
May 7, 2026

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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