Study aim: The effect of Exercise-based Cardiac Rehabilitation on the volume and size of heart valves and quality of life in myocardial infarction patients with during the COVID-19 pandemic period. Design: A clinical trial with a control group, with parallel groups and a sample size of 150 people

Study aim: This study aims to compare the effectiveness of compassion therapy and eye movement desensitization and reprocessing therapy (EMDR) on coronary anxiety, uncertainty intolerance, catastrophizing and coping efficiency of patients with coronavirus (COVID-19). Design: A clinical trial with a control group

Study aim: The objective of study is to compare the effects of Graston technique versus ischemic compression on pain, ROM of cervical spine along with functional performance among students with neck pain. Design: A randomized clinical not blind trial. Sample size 54 divided in 2 groups. Total 12 treatment sessions will be given to subjects in 4 weeks with 3 sessions/week. Settings and conduct: Setting: Sargodha Institute of Health Sciences 117-C, Zafar Ullah Road, Satellite Town Sargodha and Fatima hospital, University road, Sargodha. Participants/Inclusion and exclusion criteria: Inclusion criteria: Male and female subjects aged 18-25 years with neck pain from previous 2-3 months. Mobile phone usage >4 hours daily. Neck pain with reduced cervical range of motion (ROM).NPRS value >4 and NDI score greater than 10. Exclusion criteria: Subjects with cervical rib, migraine problem, vertebrobasilar artery insufficiency (VBI). Subjects with diagnosed cases of discogenic disease, spinal infection and inflammatory disorders, scoliosis and neck surgery or trauma. Intervention groups: Patients will be randomly divided into two groups with 27 subjects in each group. After taking baseline assessment Group A will be treated with hot pack for 7-10 min. Graston technique will be performed on neck for 5 min. On the other hand Group B will be treated with hot pack for 7-10 min. Ischemic compression approach will be performed on neck for 5 min. one set of 5 repetitions will be given.3 sessions per week on alternate days for 4 weeks treatment will be carried out. Treatment time of each session will be approximately 15 minutes. Main outcome variables: Pain(NPRS), Functional performance(NDI), Cervical AROM's(Universal Goniometer)

confirmed COVID-19 patient by RT-PCR test. Intervention groups: surgical and N95 mask, high-intensity

Study aim: The effect of using smart mobile phones on improving technophobia, mental well-being, and successful aging in elderly women isolated due to Pandemic COVID-19. Design: In order to select the samples, in the first stage, 80 elderly women will be selected from the statistical population

Study aim: The effect of “Narrative writing” on psychological health and hope in patient with covid-19 Design: A controlled clinical trial, with parallel groups, without blinding, randomized, phase 2 on 42 patients with coronary artery disease who were randomly assigned to one of the narration

Study aim: Determining the effectiveness of pregnancy self-care training application in Covid epidemic 19 on quality of life score, depression, coronary anxiety and fear of childbirth in pregnant women Design: Clinical trial with control group, with parallel groups,No blinding,Random allocation using block

Study aim: Determining the effectiveness of Methylene Blue on treatment of the Coronavirus Patients in Chaharmahal Va Bakhtiari province Design: A randomized, controlled trial, based on patients with Covid-19, which has two parallel groups. Settings and conduct: Shahrekord university of medical

Study aim: This study aims to determine the effect of tele psychologic -based mindful- parenting on anxiety and resilience of mothers of children ages 6-12 with attention deficit hyperactivity disorder (ADHD) during covid-19 outbreak Design: This study is a randomized clinical trial with two groups

Study aim: Determining the simultaneous and separate effects of 8 weeks of aerobic exercise at home and turmeric supplementation on anthropometric indices, glycemic status, lipid profile and quality of life in middle-aged women with type 2 diabetes in Kermanshah during covid-19 quarantine in 1400 Design

Study aim: Determining the Impact of a spiritual care program through virtual network on spiritual well-being and mental health of nursing internship students during the COVID-19 pandemic Design: The study is performed on 70 final year nursing students who are divided into experimental and control

Study aim: The aim of this study was to evaluate the effect of 8-weeks of aerobic training at home and vitamin D supplementation on serum levels of BDNF, NGF, fatigue and quality of life in patients with multiple sclerosis during Covid-19 quarantine. Design: For this purpose, 36 women with multiple

Study aim: The effect of garlic and cinnamon on the treatment of corona (COVID-19) patients Design: Due to the fact that no study has been done in this field so far, 45 people are divided into 3 groups of 16 people, so that from 1 to 45, it is already determined that they are a drug or placebo group

Study aim: This clinical trial aims to assess the effect of propolis on clinical symptoms in patients with coronavirus. Design: This study is a double-blind, placebo-controlled, randomized phase 2 clinical trial evaluating the effect of propolis on clinical symptoms in patients with coronavirus. In this study, 80 eligible participants will be randomly assigned to either the intervention or the control group. The randomization sequence will be generated using a random-number table. Settings and conduct: In this study, patients with coronavirus will be recruited from the Al-Zahra hospital in Isfahan. Participants who meet entry criteria will be randomly assigned to the propolis group or the placebo group. The participant's assignment will be concealed from all participants and investigators, with the exception of the study pharmacist. Participants/Inclusion and exclusion criteria: The inclusion criteria are the age of 18 to 75 years, willingness to participate with written informed consent, and the diagnosis of coronavirus based on the PCR test. The exclusion criteria are the current use of warfarin, current use of propolis supplement, and presence of sensitivity to bee products. Intervention groups: Participants in the intervention group will receive an identical propolis tablet (containing 300 mg Iranian green propolis extract) three times a day for 2 weeks. Participants in the placebo group will receive an identical tablet placebo (containing 300 mg microcrystalline cellulose ) three times a day for 2 weeks. Main outcome variables: Respiratory Rate, Chest CT scan, High-sensitivity C-reactive protein, Erythrocyte Sedimentation Rate, Severity and number of coughs

Study aim: Investigation of the effect of hesperidin use in patients with new coronavirus (COVID-19) Design: A clinical trial with a control group, with parallel, two-way blind and randomized groups on 60 patients Settings and conduct: The present study will be a randomized clinical trial and the test

milliliter; cases who diagnosed as COVID-19 infection by clinical features; laboratory findings (positive C

: Patients with covid 19 who, in addition to medication, receive thyme essential oil according to the (...) , fatigue, weakness and lethargy. Participants/Inclusion and exclusion criteria: Entry criteria: COVID 19

Study aim: The aim of this study was the efficacy of stromal vascular fractions, and also their conditioned media exosomes and blood exosomes in patients with covid-19 with acute respiratory distress syndrome /clinical trial in quality. Design: This study is a multicenter, random, double-blind study in

Exclusion Criteria: Participation in any other clinical trial of an experimental trial for COVID-19 History of taking other antivirals aginst COVID-19 in the last 24 hours at the enrollment in the study Multi

Study aim: Effect of aqueous extarct of licorice in coronavirus outpatients Design: Randomized, blinded, placebo controlled clinical trial. Effect of licorice capsules in 20 patients which have inclusion criteria will be evaluated. Simultanously, 20 patients will take placebo. Medicine and placebo in the same form and package with the alphabetics A and B will be deliverd to physiciana and patients. Patients must take the capsules three times a day for 14 days Settings and conduct: Randomized, blinded, placebo controlled clinical trial will be in mashhad . effect of licorice capsules in 20 patients with coronavirus disease which have inclusion criteria will be evaluated. Simultanously 20 patients will take placebo. Medicine and placebo in the same form and package with the alphabetics A and B will be deliverd to physician and patients. The patients must take the capsules three times a day for 14 days Participants/Inclusion and exclusion criteria: Inclusion criteria: The outpatients in quarantine, take medicine, diagnosed for coronavirus disease according to clinic ( fever, cough, myalgia) and paraclinic parameters (lymphopenia, increase CRP). Exclusion criteria: Sensitivity to licorice and it derivatives; below 18 and above 65 years old; hepato, renal or respiratory disorders; take cytotoxic, corticosteroid drugs; nursing or pregnant women Intervention groups: Effect of licorice capsules in 20 patients which have inclusion criteria will be evaluated. Simultanously 20 patients which have inclusion criteria will take placebo. Main outcome variables: Time interval until lymphopenia improves Time interval until CRP normalizes Time interval until clinical symptoms improve (fever, cough and myalgia)

Study aim: Investigation of the effect of Zufa syrup on clinical symptoms in the patients with Corona (COVID-19) Design: A randomized, controlled, Triple-blind clinical trial with 130 samples Settings and conduct: Patients who refer to the clinic that meet the study entry criteria will be selected

Study aim: Investigation effect of stress management program on psychological distress of cancer patients and caring burden and quality of life of their caregivers during the COVID-19 epidemic Design: Parallel randomized superiority controlled trial, using a random blocking allocation that cannot be blinded

Study aim: Evaluation of safety and immunogenicity of recombinant protein sub-unit COVID-19 vaccine (Razi Cov Pars) in healthy children and adolescents aged 5-17 Design: Single group, open label study (...) -PCR tests for COVID-19; Signed informed consent; Non pregnant or lactating (women); Important

Study aim: Determination the effectiveness of telenursing on the awareness and self-care performance of patients with diabetes in the conditions of the COVID-19 pandemic Design: The clinical trial has a control and intervention group, The sample size is 100 people, patient files will be selected

Study aim: Comparison of the Effect of Spinomed and Elderly Orthoses plus Back School Program and Back School Program on Physical Fitness and Respiratory Capacity of Elderly with Thoracic Kyphosis Design: A randomized, controlled, Two arm parallel group, single-blinded trial. Randomisation will be done by random digits table and 60 patient will be devided randomly to Three groups of 20 each. Settings and conduct: Location of research: Hazrate Rasoole Akram Hospital ; Sports Medicine Department ; Patients have been blinded to other groups of study Participants/Inclusion and exclusion criteria: Inclusion criteria: Age 60 years or older;Kyphosis angle 50 degrees or more ;Ability to sit and stand up and walk at least 10 meters independently Non-inclusion criteria: Physical abnormalities other than kyphosis which may need treatment prior to research or impair the research process ; People who had a history of fracture or surgery in the lower extremity or spine 12 months before the begining of the research ; Any illness or disorder that disables one's participation in exercises and group activities Intervention groups: Intervention Group 1: Spinomed Orthosis plus Back School Program Will use orthosis and exercises for 12 weeks and they will come to hospital every 2 weeks to check and improve exercises and orthoses. Then will use orthosis and exercises for 12 weeks at home. Intervention Group 2: Elderly Orthosis plus Back School Program Will use Elderly orthosis and exercises for 12 weeks and they will come to hospital every 2 weeks to check and improve exercises and orthoses. Then will use orthosis and exercises for 12 weeks at home. Control Group: Back School Program Exercises Will use exercises for 12 weeks and they will come to hospital every 2 weeks to check and improve exercises. Then will use exercises for 12 weeks at home. Main outcome variables: Physical Fitness and Respiratory Capacity