The effectiveness of desensitization with eye movements and reprocessing on the recovery of patients with COVID-19

Not Applicable

Recruiting

Conditions: COVID-19.
Personal history of COVID-19
U08.9

Registration Number: IRCT20210823052263N1

Lead Sponsor: Yasouj University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: All

Target Recruitment: 90

Inclusion Criteria

Age between 18 to 65 years old
Patients with COVID-19 who are PCR positive
Has one or more clinical symptoms including fever less than or more than 38, sore throat with or without dry cough, chills, headache, loss of taste and smell, nausea and vomiting, anorexia, diarrhea, body aches, weakness and extreme tiredness Which has no other definite justification, and spo2 = 80-93, shortness of breath, feeling of pain or pressure in the chest
No visual impairment and strabismus
No cognitive impairment such as dementia or Alzheimer's
Has no history of seizures
Has no history of known mental disorder
Not to be addicted to drugs
Patients' anxiety level should be moderate to high according to Hamilton Anxiety Questionnaire

Exclusion Criteria

The patient did not cooperate with the therapist
The patient has entered a severe phase due to pulmonary involvement and needs a niv mask or intubation

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Anxiety score in Hamilton questionnaire. Timepoint: Before intervention and after intervention. Method of measurement: Hamilton anxiety questionnaire.;Hemodynamic status (blood pressure, respiration, oxygen saturation level) with patient monitoring. Timepoint: Before intervention and after intervention. Method of measurement: Monitoring device.;Duration of hospitalization. Timepoint: Before intervention and after intervention. Method of measurement: Date of admission and discharge included in the file.

Secondary Outcome Measures

Name	Time	Method
Sleep Quality Scale. Timepoint: At the beginning of the study and one and three months after the intervention. Method of measurement: Pittsburgh Sleep Quality Questionnaire.