Clinical and Brain Effects of Remote Web-based Adapted Physical Activity (e-APA) in Patients With Psychotic Disorders and Healthy Subjects: A Controlled, Multicenter Study
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 62
- 试验地点
- 1
- 主要终点
- hippocampal volumes
研究概览
简要总结
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
详细描述
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:
- 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
- on physiological variables (neuromuscular, cardiovascular (heart rate variability) and aerobic)
- on cognitive variables by measuring working memory, episodic memory, attentional and executive functions
- on circadian rhythms (temperature, actimetry and wake-sleep cycle)
- on the clinical status of patients (severity of symptoms, quality of life, level of activity and physical abilities).
- on biological variables (fasting glucose, triglycerides, total cholesterol, High-density lipoprotein cholesterol (HDLc), Low-density lipoprotein cholesterol (LDLc)
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Be over 18 years of age and under 60 years of age
- •with schizophrenia or schizoaffective disorder according to DSM-IV (Diagnostic and Statistical Manual of Mental Disorders, 4th edition) criteria established with a semi-structured interview (Mini International Neuropsychiatric Interview, French version 5.0.0).
- •The possibility of receiving each of the 2 interventions (APA or HE)
- •No change in psychotropic drugs (antidepressants, antipsychotics or mood regulators) during the 2 months prior to inclusion for patients.
- •Collecting the signature of informed consent.
- •The need to be affiliated to a medical welfare
- •The agreement of the guardian or trustee in case of a protected major
- •Healthy Volunteers:
- •between 18 and 60 years old
- •The possibility of receiving each of the 2 interventions (APA or HE)
- •Collecting the signature of informed consent.
- •The need to be affiliated to a medical welfare
排除标准
- •Patients with only one of the non-inclusion criteria may not be eligible to participate in the research. These criteria are:
- •Age under 18 or over 60 years old
- •Pregnancy
- •The inclusion of the patient in another biomedical research protocol (during the present study)
- •Patients with progressive neurological disease
- •Patients with contraindications to MRI (including electronic or metal implants)
- •Patients who refused to wear earplugs during the MRI examination
- •Patients with a physical contraindication to physical activity (moderate to severe heart failure, severe valvular disease, unstable coronary disease, acute pulmonary embolism or untreated deep venous thrombosis, uncontrolled hypertension, pulmonary arterial hypertension, treaty)
- •Neuromuscular pathologies, severe sensory and / or motor neuropathy
- •Rheumatic and articular pathologies; Rheumatologic / orthopedic problems or bone lesions at risk of fracture contraindicating physical activity
- •History of stroke or myocardial infarction less than 6 months old at the selection visit
- •Healthy Volunteers
- •Participants with only one of the non-inclusion criteria may not be eligible to participate in the research. These criteria are:
- •Age under 18 or over 60 years old
- •Pregnancy
- •Inclusion of the participant in another biomedical research protocol (during this study)
- •Participants with progressive neurological disease
- •Participants with a contraindication to MRI (including electronic or metal implants)
- •Participants refused to wear ear plugs during the MRI examination
- •Participants with life-long schizophrenia or schizoaffective disorder according to the DSM-IV criteria established with a semi-structured interview (Mini International Neuropsychiatric Interview, MINI; French version 5.0.0).
- •Presence of cardiovascular pathologies contraindicating physical activity (moderate to severe heart failure, severe valvular disease, unstable coronary disease, acute pulmonary embolism or untreated deep venous thrombosis, uncontrolled hypertension, pulmonary arterial hypertension, rhythm disorder untreated)
- •Neuromuscular pathologies, severe sensory and / or motor neuropathy
- •Rheumatic and articular diseases, rheumatological / orthopedic problems or fracture risk bone lesions
- •History of stroke or myocardial infarction less than 6 months old at the selection visit
研究组 & 干预措施
APA in patients
patients receiving physical activity (APA) by web during 16 weeks with 2 sessions a week
干预措施: Physical activity (APA) (Behavioral)
HE in patients
patients receiving Health education program (HE) by web during 16 weeks with 2 sessions a week
干预措施: Health Education program (HE) (Behavioral)
APA in healthy volunteer controls
Healthy volunteers receiving physical activity (APA) by web during 16 weeks with 2 sessions a week
干预措施: Physical activity (APA) (Behavioral)
HE in healthy volunteer controls
Healthy volunteers receiving Health education program (HE) by web during 16 weeks with 2 sessions a week
干预措施: Health Education program (HE) (Behavioral)
结局指标
主要结局
hippocampal volumes
时间窗: at Day 127 +/- 8 days or after 10 sessions of APA if premature cessation of treatment
The primary endpoint is the right and left hippocampal volumes
次要结局
- Cerebral variables(at Day 127 +/- 8 days or after 10 sessions of APA if premature cessation of treatment)
- Physiological variables(at Day 127 +/- 8 days or after 10 sessions of APA if premature cessation of treatment)
- Circadian rhythms(at Day 127 +/- 8 days or after 10 sessions of APA if premature cessation of treatment)
- Clinical status(at Day 127 +/- 8 days or after 10 sessions of APA if premature cessation of treatment)
- Biological variables(at Day 127 +/- 8 days or after 10 sessions of APA if premature cessation of treatment)