Actively Recruiting
A Mixed Intervention to Improve Resilience for Patient With Neurocognitive Disorders
Led by Centre Hospitalier Universitaire de Nice · Updated on 2025-05-04
90
Participants Needed
1
Research Sites
135 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The study aims to test a program combining cognitive behavioral therapy techniques, positive psychology techniques, mindfulness meditation and yoga, in order to improve resilience in patient with minor cognitive disorder. This intervention will be compared to a control group, but also with a group testing another intervention (an intervention that does not improve resilience in the elderly, namely a "cognitive stimulation" intervention) in order to ensure that the effect potentially obtained is not due to the simple management of the participant. The duration of the intervention will be 3 months, with an evaluation directly before and after the intervention. In addition, in order to best evaluate the effectiveness of the interventions over time, two follow-up measurements will be proposed: a measurement one month after the intervention, then a final one three months after the intervention.
CONDITIONS
Official Title
A Mixed Intervention to Improve Resilience for Patient With Neurocognitive Disorders
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Man or woman aged > 60 years
- Diagnosed with a minor neurocognitive disorder according to DSM 5 criteria
- Score of 145 or less on the Wagnild and Young Resilience Scale
- Able to read and write French
- Beneficiary of a social security scheme
- Able to understand and sign free and informed consent
You will not qualify if you...
- Currently practicing meditation, yoga, or Tai Chi
- Currently undergoing psychological therapy
- Major hearing, visual, or motor disability interfering with interventions or assessments
- History or presence of major psychiatric disorders within the last 5 years
- Psychotropic treatment dose not stable for at least 4 weeks
- Vulnerable persons as defined in Articles L1121-5 to -8
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
CHU de Nice
Nice, France, 06003
Actively Recruiting
Research Team
L
LEMAIRE JUSTINE
CONTACT
F
foussat valérie
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
3
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here