Study aim: Overall Objective: To evaluate the effectiveness of resilience training on coping styles in hardworking personnel (steel company) and their spouses in coronary conditions Minor Objectives: 1. Assessing the coping styles of steel personnel and their spouses in the context of the Corona epidemic 2. Assessing the resilience of steel personnel and their spouses after interventions 3- Determining the effectiveness of resilience training on coping styles in steel company personnel and their spouses Design: The present study is a quasi-experimental study in which a pre-test-post-test design with a control group will be used. The statistical population of this research will include all married personnel of Kavir Steel Company in Aran and Bidgol in 1401. Then, 30 pairs will be randomly selected from these individuals and will be placed in two experimental (15 pairs) and control (15 pairs) groups. Settings and conduct: Aran and Bidgol Steel Company Participants/Inclusion and exclusion criteria: All married staff of Kavir Steel Company of Aran and Bidgol cities Criteria for entering this study include 1- No history of mental illness and hospitalization in mental hospitals 2- Willingness to participate in the research through interviews. Exclusion criteria are 1- Absence from more than one training session 2- Simultaneous participation in other psychotherapy programs. A resilience component training program (Henderson and Milleston, Krotz 1997) will be used. The experimental group will receive one training session in 8 sessions of 1 hour per week, but the control group will not participate in these sessions. Intervention groups: resilience training course, Main outcome variables: resilience enhancing

Study aim: Determining the effectiveness of mindfulness-based cognitive therapy on anxiety of treatment staff in contact with COVID_19. Determining the effectiveness of mindfulness-based cognitive therapy on the components of burnout in medical staff in contact with COVID_19. Design: The study will be done in two groups, a control group and an experimental group. The subjects will be selected voluntarily but the assignment in the two groups will be done randomly with a lottery table. The total number of subjects will be 40 who will be divided into two groups. Settings and conduct: Therapy will be done through the Skype program, eight one-hour sessions. All pre-tests and post-tests will be done through the PorsLine link or manual forms. Participants/Inclusion and exclusion criteria: Admission requirements: conscious satisfaction; obtaining a score above 15 in the Beck Anxiety Questionnaire; optimal physical and mental condition to participate in the study; there is no specific age limit. Exclusion criteria: simultaneous receipt of other psychological or pharmacological interventions؛ at least two weeks before the start of the intervention; change of the subject's opinion about participating in the study. Intervention groups: Mindfulness-based cognitive therapy is performed virtually on Skype in eight one-hour sessions one week apart. For the control group, the same treatment will be performed after the end of the study. Main outcome variables: Anxiety; job burnout

Study aim: Comparing the effectiveness of acceptance and commitment therapy and hope therapy based on a positive psychology approach on psychological well-being and improving the mental health of medical staff during the covid-19 epidemic Design: Clinical trial, with control group, with parallel

with a diagnosis of septic shock is admitted to the intensive care unit; No covid-19 disease (negative

infectious disease such as Covid 19; Patients older than 70 years or less than 30 years; Patients with low

Study aim: To determine the effect of using the mask with an innovative nutritional adaptor on the nutritional status of the patient with COVID-19 Design: crossover RCT design was employed to achieve the (...) phase*Patient diagnosis covid-19*Intensive care patient*Patient on CPAP mask*Conscious*Adult patient

Study aim: The aim is to improve students upper body posture in online learning conditions at home, reduce pain / discomfort caused by these conditions and raise students' level of awareness and attitude towards prevention. Design: A clinical trial with a control group, with parallel, randomized groups, will be performed on 180 students. Settings and conduct: In order to identify students with forward head deformity , due to the lack of physical access to students online, asks students if they feel this anomaly to more accurately evaluate and Maintaining a healthy protocol at the specified days and hours refer to the Corrective exercise center. Participants/Inclusion and exclusion criteria: Criteria for entering the exercise: 1. High school students 2. Having musculoskeletal disorders 3. Having forward head deformity with an angle higher than 45 degrees Exclusion criteria: 1. History of vertebral surgery 2. Back tumor 3. History of fractures in the cervical spine 4. Osteoporosis 5. Dissatisfaction with participating in exercises Intervention groups: Individuals with musculoskeletal disorders and head-forward abnormalities were identified and after selecting the samples, subjects were divided into 3 groups of individuals with musculoskeletal disorders (exercise-ergonomic advice group, ergonomic advice group and control group) and 3 groups of individuals with head-to-head abnormalities. The front (exercise group - ergonomic advice, ergonomic advice group and control group) will start training for 8 weeks. All exercises are performed online by a corrective exercise specialist. Main outcome variables: 1- Improving students' upper body posture in online learning conditions at home 2- Reducing pain / discomfort caused by these conditions

Study aim: Study the effect of one shot cognitive behavioral therapy on insomnia and heart rate variability of health care workers at the time of Covid-19 pandemic Design: Clinical trial, with parallel groups, for 70 patients, randomized using a random string, double-blind, the outcome evaluator and data

Study aim: A randomized, crossover bioequivalence study of single dose of test formulation (one tablet of Favipiravir 200mg tablet of Actover Co., IRAN) in comparison of reference product (one tablet of Avigan 200mg tablet of Toyoma Chemical) by means of AUC0-t and Cmax in healthy adult human subjects under fasting conditions. Design: A randomized, open label, single dose, crossover, bioequivalence study in 24 healthy subjects under fasting condition Settings and conduct: This study is carried out in Core Research Center of Zahedan University of Medical Sciences located in Imam Ali Hospital in Zahedan. There is a separate space for sampling and forecasting emergency situations in order to accommodate and rest the volunteers. This crossover and open label study was performed on 24 healthy volunteers. The volunteers' health is verified by the project physician prior to entry into the study, and the volunteers' status is regularly monitored by the project physician on the day of drug administration. This study will be covered by insurance in order to compensate for any adverse effects. Participants/Inclusion and exclusion criteria: Main Inclusion criteria: Healthy subjects aged between 18 -50 years old and weighted between 50 – 100 kg\\ Main exclusion criteria: Clinically relevant deviations from normal; Donation a unit of blood or participated in another clinical trial within the last two months; History of drug or alcohol abuse; Used any medication within 7- 14 days before the first treatment; Intervention groups: Intervention: Single dose of one Favipiravir 200mg tablet of Actover Co, IRAN Control: Single dose of one Avigan 200mg tablet of Toyoma Chemical Main outcome variables: Plasma concentration of favipiravir at 0 (before dosing), 0.25, 0.5, 0.75, 1.0, 1.5, 2.0, 2.5, 3.0, 4.0, 6.0, 8.0 &10.0hr. after dosing

lavender allergy (dermal or inhalation) Covid 19 disease based on PCR test results Have a history of

Study aim: Determining the effects of melissa officinalis on stress, anxiety, depression, sleep disorders and compassion fatigue among Nurses Caring for COVID-19 Patients Design: Clinical trial with control group, with parallel groups, double-blind, randomized, phase three on 88 nurses, for randomization

Study aim: Effect of medroxyprogesterone vs Placebo on Duration of Non-invasive Mechanical Ventilation Among Patients With COPD Design: The study is a parallel randomized phase 2, double-blind, placebo-controlled clinical trial. One hundred COPD Patients who admitted to Rahnemoun Hospital will be randomized to each of the groups using a random number table (50 patients per group). Patients will receive six tablets of medroxyprogesterone or placebo daily for ten days. The steps will be covered from the perspective of the patient, the treating physician, and the assessors. The first presenter identifies the sequence of assignments of patients according to the order of entry of the patients into the study, puts the tablets into one-size boxes for patient use, and identifies them with A or B codes. Settings and conduct: Patients with COPD who admit to Rahnemoun Hospital will be randomized to each of the groups using random number table. Patients will receive six tablets of medroxyprogesterone or placebo daily for ten days. The steps will be covered from the perspective of the patient, the treating physician, and the assessors. The first presenter puts the tablets into one-size boxes for patient use, and identifies them with A or B codes. Participants/Inclusion and exclusion criteria: Inclusion criteria included pH <7.25 <7, PCO2≥50 mmHg, GCS> 8, no severe drowsiness, and patients will be excluded from the study if they have any of the following: cystic fibrosis or disseminated bronchiectasis, history of medroxyprogesterone allergy, severe heart, liver, or kidney failure use of NIV at home Intervention groups: One group is the Medroxy Progesterone recipient, the other is the placebo recipient. Main outcome variables: Mortality rate, duration of ventilation, length of stay in intensive care unit and hospital, clinicalstatus of patients, hospital discharge, scorpion sofa and GCS.

Study aim: Study the effect of online visual games on balance, visual perception, and oculomotor skills of children with developmental dyslexia during Covid -19 pandemic Design: The interventions will be designed and made by Niloufar Chamani (Master of Sciences student in Occupational Therapy) as

Study aim: The aim of this study was to evaluate the effect of Tadalafil administration in accelerating the recovery process of erectile dysfunction caused by COVID 19 disease. Design: A clinical trial with a control group, with parallel, double-blind, randomized groups performed on 60 patients

Study aim: Determining the effect of semi-sitting position (group A (, tripod (group B)) and lower back (group C) on vital signs and comfort pattern in patients with COVID19 Design: In this clinical trial, 90 eligible patients will be selected and placed in three groups A, B, C. This study will be performed on three groups, one control group and two intervention groups. The study is double-blind with parallel groups, randomized. In this study, phase is not applicable. Rand function in Excel software will also be used for randomization. Settings and conduct: This study will be performed in Amir Al-Momenin Hospital in Arak. Participants' expert and sample collector do not know how to randomize. Participants/Inclusion and exclusion criteria: Inclusion criteria: Infection by coronavirus (positive PCR test), age 20 to 70 years, willingness to participate in research, lack of connection to a mechanical ventilator (no intubation), ability to communicate, no underlying respiratory disease, no pregnancy, No history of abdominal surgery during the last 6 months (for placement in the lumbar position), having lung involvement of at least 10% with shortness of breath Exclusion criteria: patient death, unwillingness to participate in further research, patient intubation during research, abdominal obesity, abdominal surgery recently Intervention groups: Patients admitted to corona wards to measure the effect of three semi-sitting , tripod and prone positions on vital signs and patients' comfort pattern. Main outcome variables: Improve vital signs and comfort pattern

Study aim: Determining the effect of education on the quality of nutrition of hemodialysis patients in the prevalence of COVID-19. Design: Clinical trial with intervention and control groups, with parallel groups, one-way blind, randomized, because the drug was not used in this study, the trial phase is

Study aim: The Effictiveness of mobile application Positive Psychological Intervention (PPI) on Improving Well‑Being Among Students of Hamadan Universities during Corona Virus Pandemic. Design: A, controlled clinical trial with a parallel-group design of 252 students, who will be registered and studied and will be followed for three months. Settings and conduct: This study will be conducted in the universities of medical sciences, Islamic Azad in Hamadan City. The sample number is 252 students who will be assigned to intervention groups (intervention and control) by cluster method. The intervention includes fourteen application-based education sessions. The intervention is performed at the universities of the experimental group and three months after the intervention, the questionnaires are completed again and the data obtained from the two groups are analyzed and compared. Participants/Inclusion and exclusion criteria: Inclusion criteria also include student enrollment in hamadan universities; Desire to participate in the study (completing the consent form, completing the questionnaire), and having completed at least one semester of the student's education at the mentioned university. Exclusion criteria include students who are unable to respond and participate in the study and have a mental illness under psychological counseling elsewhere, suffering from mental illness; Depression and the use of anti-stress and anxiety medications are noted. Intervention groups: Students of universities in Hamadan will include students of the University of Medical Sciences, Islamic Azad University of Hamadan . Main outcome variables: Changes in flourishing scores, measuring depressive symptoms, and fear of covid19 scores

with a non-heparin anticoagulant 11) Covid-19 Infection Intervention groups: Thirty patients with

Study aim: Determining the effectiveness of acupuncture grief in improving the respiratory symptoms of hospitalized patients with coronavirus Design: A controlled randomized clinical trial, single blinded, phase 3 on 18 patients, using Random Allocation Software for randomization Settings and conduct: Samples include patients with coronavirus who are hospitalized in Ali Asghar Hospital in Shiraz. To blind the clinical evaluator, the study groups are named A and B. Participants/Inclusion and exclusion criteria: Inclusion criteria: The patient's corona virus is approved by PCR test The patient is hospitalized, The patient agrees to participate in the study, The respiratory rate of the patient is more than 30 times per minute, Blood oxygen level should be less than 93%, The patient have pulmonary infiltration according to chest x-ray graph, The patient does not afflict from any serious simultaneous heart, lung, brain, and endocrine disease, Exclusion criteria: The patient suffers from any serious concomitant diseases of the heart, lungs, brain, glands, Patient dissatisfaction with participation in the study, Pregnant and lactating mothers, Existence of any conditions in the patient that, according to the physician's judgment, prevent the continuation of the treatment intervention, Resistant hypoxemia, Hemodynamic instability, Hypercapnia Intervention groups: In intervention group ghamz with needle will be performed at six points LU5, LU7 and SP6, bilaterally for 20 minutes daily for 7 days. In control group sham therapy will be performed at six points LU5, LU7 and SP6, symmetrically on both sides of the body, (points 5 and 7 of the lung path and point 6 of the spleen path) for 20 minutes daily for 7 days. patients in both groups receive conventional medical treatments. Main outcome variables: Vital signs and respiratory symptoms of the patient

healthcare workers in hospitals aging 18 to 59 who have been in contact with COVID-19 patients and suffering

with COVID 19 By receiving oxygen by reserve bag, they have less than 93% oxygen saturation Provided

Study aim: Assessment The effect of resveratrol supplementation on some inflammatory factors in patients with severe COVID19 Design: This study is a two arm parallel groups clinical trial that will be done in Ahvaz hospital. Randomization is done through block method. Sample size of this study is 60 patients that divided equally into two groups include intervention and control groups .This is a phase 3 clinical trial. Settings and conduct: This study is a two arm parallel groups clinical trial that will be done in Ahvaz hospital. In this study, blindness is not performed. Participants/Inclusion and exclusion criteria: Inclusion criteria: chain reaction (PCR) confirmed infection with COVID19 ; Lung involvement confirmed with chest imaging; Hospitalized with: Fever (axillar or oral temperature ≥ 38.0 °centigrade(C) or ≥38.6°centigrade tympanic or rectal) or respiratory rate >24/min or cough; Less than 8 days since illness. Non-inclusion criteria: Autoimmune diseases (lupus, MS, etc.); Hepatic failure; Hepatit B, C; pregnant and lactating women Intervention groups: Both case and control group will be received routine drugs. 1. Intervention group: Resveratrol produced by Sumabe company, one Tab, daily until 14 days. 2. control group: received routine drugs. Main outcome variables: Time to clinical recovery, respiratory signs, Intubation rate.

Positive findings of PCR or CT scan based on COVID-19 disease Tendency to attend a clinical trial study The

Study aim: Effect of Benson Relaxation on Quality of Life and job stress in nurses in intensive care units with Covid-19 pationts Design: This study was a clinical trial with control group with parallel design. The sample size of 65 patients was randomly divided into two equal groups. Settings and

conduct: Before COVID-19 Outbreak : two sections have been held in hospital, each section 2 hours a day. After COVID-19 Outbreak and limitations : six sections have been held online. Participants/Inclusion