Condition 1: Stress. Condition 2: Anxiety. Condition 3: depression. Reaction to severe stress, unspecified Generalized anxiety disorder Depressive episode, unspecified
Conditions
Interventions
Intervention 1: In the control group patients will receive standard care. If the effectiveness of the intervention is proved, after a study of the control group as well as methods of controlling anxie
s/he will explain the purpose of the intervention for patients
then, information about the nature of the symptoms and course of anxiety, stress and depression will be given to them. In the second session, their questions are answered. The successful experiences o
such as physical activity, weight control, diet, activity level social routine and follow-up treatment.
Treatment - Other
In the control group patients will receive standard care. If the effectiveness of the intervention is proved, after a study of the control group as well as methods of controlling anxiety, stress and d
In the intervention group, training is done in three sessions during 45 minutes for each of them by peers. In the first session, patients will introduce to each other while they meet with peer researc
Sponsors
Qom University of Medical Sciences
Eligibility
Sex/Gender
All
Age
60 Years to 90 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: being aware of time, place and person; The patient should be able to understand the contents in the Persian language; s/he should not have the history of proven mental diseases; s/he should not have severe visual and hearing disorders; s/he should have full consent for the study; s/he should not have consume anti-depressants and anti-anxiety drugs; s/he should not took apart in stress training courses over the last 6 months. Exclusion criteria: Occurrence of unexpected events for the patient during the study (Patient dies); s/he should not have the desire to continue the clinical working trial.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Anxiety. Timepoint: Before intervention, 24 hours after treatment and one month after intervention. Method of measurement: DASS 21 questionnaire.;Stress. Timepoint: Before intervention, 24 hours after treatment and one month after intervention. Method of measurement: DASS 21 questionnaire.;Depression. Timepoint: Before intervention, 24 hours after treatment and one month after intervention. Method of measurement: DASS 21 questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contactkurosh jodaki
Qom University of Medical Sciences
Outcome results
None listed