chronic pain.
Conditions
Interventions
Intervention 1: Intervention group: The electronic content will be available to family caregivers in a period of 8 weeks. This content includes training manuals for caring for patients with chronic pa
Sponsors
Shiraz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Entry conditions for family caregivers of patients with chronic pain and their patients: - Literacy in reading, writing and speaking in Persian language - According to the doctor's diagnosis, the patient has had chronic pain for at least 3 years -Having a smart mobile phone and the ability to work with it - A caregiver who has been taking care of the patient for the past 3 months and lives with the patient. - Willingness to participate in the study
Exclusion criteria
Exclusion criteria: Exclusion criteria of family caregivers of patients with chronic pain and their patients from the study: - Unwillingness to continue participating during the study - The occurrence of unfortunate events for relatives of caregivers and patients (severe mental or physical illness) and events such as accidents, divorce, death, etc.) during the study - Caregiver participating in psychotherapy programs or receiving psychological counseling in the last 6 months - Diagnosis of cancer or any other chronic disease other than pain in patients during the study - Hospitalization of the patient and receiving psychological interventions during the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Caregivers' quality of life. Timepoint: before the start of the intervention, immediately after the end of the intervention and three months after the end of the intervention. Method of measurement: ???????? ????? ????? ??????? ??? ? ?????.;Caregiver general self-efficacy. Timepoint: before the start of the intervention, immediately after the end of the intervention and three months after the end of the intervention. Method of measurement: Scherer and Maddox general caregiver self-comedy questionnaire.;Caring load, careful. Timepoint: before the start of the intervention, immediately after the end of the intervention and three months after the end of the intervention. Method of measurement: Questionnaire of caregiving burden, caregiving Novak and Gast. | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of life of patients with chronic pain. Timepoint: before the start of the intervention, immediately after the end of the intervention and three after the end of the intervention. Method of measurement: World Health Organization Quality of Life Questionnaire.;Pain-induced self-efficacy of patients with chronic pain. Timepoint: before the start of the intervention, immediately after the end of the intervention and three after the end of the intervention. Method of measurement: Nicholas' pain self-efficacy questionnaire.;Pain-induced disability in patients with chronic pain. Timepoint: before the start of the intervention, immediately after the end of the intervention and three after the end of the intervention. Method of measurement: Questionnaire of disability due to pain in patients with chronic pain Roland and Morris. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMaryam Shaygan
Shiraz University of Medical Sciences
Outcome results
None listed