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the effect of virtually designed resilience improvement program on outcomes of chronic pain patients

Investigation the effect of virtually designed resilience improvement program on outcomes of chronic pain patients referred to Shiraz University of Medical Sciences affiliated clinics

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210719051944N1
Enrollment
105
Registered
2021-10-31
Start date
2022-05-22
Completion date
Unknown
Last updated
2021-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chronic pain. Chronic pain syndrome

Interventions

Intervention 1: Intervention group: In addition to routine care, a "virtualized resilience promotion program" will be implemented for patients in this group. the educational contents will be sent to t

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age >18 years Diagnosis of chronic pain according to ICD-11 criteria (all types of non-cancerous chronic pain), according to the patient's report Willingness to participate in the study Literacy of reading, writing and speaking in Persian Having a smart phone with WhatsApp social network and the ability to work with it Internet access

Exclusion criteria

Exclusion criteria: Having other chronic physical diseases such as cancer and MS, according to the patient's own report Known chronic mental illness, according to the patient's own report Diagnosis of cancer or any other chronic disease (such as MS) during the study Occurrence of adverse events for the patient's relatives (severe mental or physical illness) such as accident, divorce, death, etc. during the study Unwillingness to continue participating during the study Participate in psychotherapy programs or receive psychological counseling in the last 6 months

Design outcomes

Primary

MeasureTime frame
Resilience level in CD- resilience questionnaire. Timepoint: before intervention, immediately and 3 mounts after intervention. Method of measurement: CD- resilience questionnaire.

Secondary

MeasureTime frame
Pain intensity. Timepoint: before intervention, immediately and 3 mounts after intervention. Method of measurement: numeric rating scale.;Pain disability. Timepoint: before intervention, immediately and 3 mounts after intervention. Method of measurement: pain disability index.;Psychological wellbeing. Timepoint: before intervention, immediately and 3 mounts after intervention. Method of measurement: Ryff psychological wellbeing questionnaire (short form).;Social wellbeing. Timepoint: before intervention, immediately and 3 mounts after intervention. Method of measurement: Keyes social wellbeing questionnaire (short form).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Niloofar Pasyar

Shiraz University of Medical Sciences

pasyarn@yahoo.com+98 71 3647 4254

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026