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临床试验/NCT06815484
NCT06815484已完成不适用

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

GCS Ramsay Santé pour l'Enseignement et la Recherche2 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2025年3月12日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
75
试验地点
2
主要终点
Shirom - Melamed Burnout Measure

研究概览

简要总结

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).

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Investigator)

盲法说明

The choice of randomisation by minimisation allows participants to be allocated at random to the two groups (intervention and control groups), thus ensuring a balance in the known characteristics likely to influence the results.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • 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.

研究组 & 干预措施

Intervention group : adaptive physical activity programme

Experimental

Participants will benefit from an adaptive physical activity programme supervised by a physical activity professional over a 9-week period. Participants will also receive 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.

干预措施: Intervention group with physical activity programme (Other)

Intervention group : adaptive physical activity programme

Experimental

Participants will benefit from an adaptive physical activity programme supervised by a physical activity professional over a 9-week period. Participants will also receive 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.

干预措施: Recommendations of the World Health Organisation (Other)

Control Group : recommendations on physical activity

Active Comparator

Participants will be given only the World Health Organisation's recommendations on physical activity. At the end of the 9-week intervention period, participants will have the opportunity to take part in a motivational interview with a physical activity professional to encourage regular physical activity.

干预措施: Recommendations of the World Health Organisation (Other)

结局指标

主要结局

Shirom - Melamed Burnout Measure

时间窗: 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.

次要结局

未报告次要终点

研究者

发起方
GCS Ramsay Santé pour l'Enseignement et la Recherche
申办方类型
Other
责任方
Sponsor

研究点 (2)

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