Feasibility of Stress Management Education Delivered Via Virtual Classroom in Nursing Homes: a Pilot Study of a RCT

Last updated: March 10, 2025
Sponsor: GCS CIPS
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

Stress management

Clinical Study ID

NCT06727682
AGIT-RESTS-1
  • Ages > 18
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

The aim of this cluster-randomised pilot study is to assess the feasibility of a remote stress management programme to reduce occupational stress in healthcare workers in specialised care units of nursing homes. Secondary aims are to assess the effectiveness of the programme in reducing stress in care workers and reducing behavioural and psychological symptoms of dementia in residents.

Participants randomised to the experimental cluster will follow the stress management programme delivered in a virtual classroom. Participants randomised to the control cluster will be placed on a waiting list.

The primary outcome measure will be the participation rate in the study. Other secondary outcomes will include measures of heart rate variability (as a marker of physiological stress) and scores on specific questionnaires for stress, anxiety and risk of burnout in nursing staff in the specialised care units, and behavioural and psychological symptoms of dementia and quality of life in residents in the specialised care units.

Both clusters will complete the same assessments. Participants in the experimental cluster will follow a three-course programme with a psychologist via videoconferencing over a period of 2 months. After the study's final evaluation visit, which will take place one month after the programme, participants in the control cluster will be offered the opportunity to follow the same programme.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Having a caring relationship with residents (e.g. nurses, nursing assistants)

  • Working in the specialised care unit of the nursing home

  • Working in the nursing home for at least 3 months on the date of inclusion and whoseemployment contract does not end within 3 months of the date of inclusion.

  • Obtaining express written informed consent, after a period of reflection

Exclusion

Exclusion Criteria:

  • Person in a period of relative exclusion in relation to another protocol

  • Person who is not affiliated to or does not benefit from a social security scheme.

  • Pregnant or lactating woman

  • Participant unable to give consent

  • Person deprived of liberty by judicial or administrative decision

  • Person unable to understand, speak, read and write French

Study Design

Total Participants: 40
Treatment Group(s): 1
Primary Treatment: Stress management
Phase:
Study Start date:
December 02, 2024
Estimated Completion Date:
April 30, 2025

Connect with a study center

  • Korian Parc de l'abbaye

    Saint-Cyr-l'École, Ile-de-France 78210
    France

    Active - Recruiting

  • Korian Parc des dames

    Saint-Germain-en-Laye, Ile-de-France
    France

    Active - Recruiting

  • Korian Le Clos de l'orchidée

    Narbonne, Occitanie 11100
    France

    Active - Recruiting

  • Korian La Colombe

    Gigean, 34770
    France

    Active - Recruiting

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