ClinConnect ClinConnect Logo
Search / Trial NCT07058389

Synergy Between Physical Activity and Outdoor Green Environments to Reduce the Intensity of Negative Symptoms in Schizophrenia.

Launched by CENTRE HOSPITALIER UNIVERSITAIRE DE SAINT ETIENNE · Jul 7, 2025

Trial Information

Current as of July 22, 2025

Not yet recruiting

Keywords

Schizophrenia Disorders Mental Health Quality Of Life Physical Fitness

ClinConnect Summary

This clinical trial is exploring whether doing physical activity outdoors in green, natural environments can help reduce the negative symptoms of schizophrenia more effectively than exercising indoors. Negative symptoms include things like feeling less motivated, having less interest in activities, or showing less emotion. The study is based on the idea that being active is good for mental health, and being surrounded by nature might make exercise even more helpful for people with schizophrenia.

To take part, individuals need to be between 18 and 55 years old, have a diagnosis of schizophrenia with ongoing negative symptoms, and be regularly followed by a psychiatrist. Participants should be physically able to do exercise safely and have no serious joint, heart, or neurological problems. Pregnant women and people who drink a lot of alcohol or caffeine won’t be able to join. Those who participate will be asked to exercise either outdoors in green spaces or indoors, and researchers will see how this affects their symptoms and overall well-being. The study is not yet recruiting, but it hopes to provide new insights into how combining physical activity with nature might improve life for people living with schizophrenia.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patients with schizophrenia, aged 18 to 55 years
  • Having persistent negative symptoms (SNS), negative symptoms self-assessment scale \> 7
  • Regularly monitored in the psychiatry department.
  • Have no medical contraindications to physical activity
  • Subject affiliated with or entitled to a social security system.
  • Subject having received informed information about the study and having co-signed, with the investigator, consent to participate in the study.
  • Male or female.
  • Exclusion Criteria:
  • Patient unsuitable for study in the opinion of the investigator
  • Any subject with chronic joint pathologies (example: repeated sprains, patellar or ligament problems) or cardiac pathologies.
  • Any subject presenting chronic or central neurological pathologies.
  • Any subject deprived of liberty or subject to legal protection
  • Excessive consumption of alcohol (\> 14 glasses per week) or caffeinated drinks (\> 400 mg of coffee per day).
  • Pregnant women.
  • Subject unable to understand the purpose and conditions of the study, unable to give consent.

About Centre Hospitalier Universitaire De Saint Etienne

The Centre Hospitalier Universitaire (CHU) de Saint-Étienne is a leading academic medical center in France, dedicated to advancing healthcare through innovative clinical research and high-quality patient care. With a robust infrastructure that supports a wide range of medical specialties, CHU de Saint-Étienne fosters collaboration between healthcare professionals, researchers, and academic institutions. The center is committed to conducting rigorous clinical trials that adhere to ethical standards and regulatory requirements, aiming to improve treatment outcomes and enhance the overall health of the community. Through its dedication to scientific excellence and patient-centered care, CHU de Saint-Étienne plays a pivotal role in the advancement of medical knowledge and the development of new therapeutic interventions.

Locations

Saint Etienne, , France

Patients applied

0 patients applied

Trial Officials

Medhi HOUSNI, Md

Principal Investigator

CHU de Saint-Etienne

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported