A Controlled Study With Remote Web-based Adapted Physical Activity (e-APA)

Status Terminated

Clinical Trial Summary

In this study, an APA program by web (e-APA) will be offered to two groups of participants (21 patients and 21 healthy volunteers (HV)) in remote video (use of the SAPATIC (Santé Activités Physiques Adaptées utilisant les Technologies de l'Information et de la Communication) platform developed by the company V@SI). At the same time, two control groups, a group of 21 patients and a group of 21 HV will undergo an health education program (HE) through the collaborative SAPATIC health platform of V@Si and will constitute the control groups. The content of the APA sessions will be administered by V@Si. This program offers content aimed to improve aerobic capacity and muscular strength while relying on the motivation of the participants

Clinical Trial Description

The main objective is to demonstrate that APA can improve cerebral plasticity in patients with schizophrenic or schizoaffective disorders (SCZ), reflected by an increase in the overall volume of hippocampus. The secondary objectives will also be to assess the impact of APA on the SCZ compared to the HV: 1. on other cerebral variables (changes in the different subregions of the hippocampus (Cornu Ammonis (CA: CA1,CA2-3-4), subiculum and dentate gyrus), cortical thickness, N-acetyl aspartate (NAA) and glutamate as well as changes in the white matter through the diffusion markers (fractional anisotropy, radial diffusivity and mean diffusivity in the frontomedial-hippocampal fibers) and cerebral irrigation 2. on physiological variables (neuromuscular, cardiovascular (heart rate variability) and aerobic) 3. on cognitive variables by measuring working memory, episodic memory, attentional and executive functions 4. on circadian rhythms (temperature, actimetry and wake-sleep cycle) 5. on the clinical status of patients (severity of symptoms, quality of life, level of activity and physical abilities). 6. on biological variables (fasting glucose, triglycerides, total cholesterol, High-density lipoprotein cholesterol (HDLc), Low-density lipoprotein cholesterol (LDLc) ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03261817
Study type	Interventional
Source	University Hospital, Caen
Contact
Status	Terminated
Phase	N/A
Start date	September 29, 2017
Completion date	June 22, 2021

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

A Controlled Study With Remote Web-based Adapted Physical Activity (e-APA) in Psychotic Disorders — PEPSYV@SI

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms