The effect of mobile-based pain control education on the pain and quality of life of adolescents with chronic pain in Shiraz

The effect of mobile-based pain management education on the pain and quality of life of adolescents with chronic pain in Shiraz, 1397

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180808040744N2

Enrollment

640

Registered

2019-04-12

Start date

2019-02-20

Completion date

Unknown

Last updated

2019-04-23

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

Conditions

chronic pain. Chronic pain, not elsewhere classified

Interventions

Intervention 1: First intervention group: In the mobile-based education group, the software will provide educational materials to the patients. For this purpose, patients in this group receive weekly

Eligibility

Sex/Gender

All

Age

12 Years to 18 Years

Inclusion criteria

Inclusion criteria: Age between 12 to18 years Secondary education Access to smart phone Having chronic pain diagnosis based on ICD 11 criteria

Exclusion criteria

Exclusion criteria: According to a person, he has chronic mental illness According to one's own opinion, the presence of other non-painful physical, chronic physical illnesses

Design outcomes

Primary

Measure	Time frame
Quality of life score in pediatrics quality of life questionnaire. Timepoint: At the beginning of the study, immediately and 3 months after the end of the intervention. Method of measurement: Pediatrics Quality of life questionnaire.;Pain severity score in pain intensity questionnaire. Timepoint: At the beginning of the study, immediately and 3 months after the end of the intervention. Method of measurement: Numeic rating scale questionnaire.	—

Measure

Time frame

Quality of life score in pediatrics quality of life questionnaire. Timepoint: At the beginning of the study, immediately and 3 months after the end of the intervention. Method of measurement: Pediatrics Quality of life questionnaire.;Pain severity score in pain intensity questionnaire. Timepoint: At the beginning of the study, immediately and 3 months after the end of the intervention. Method of measurement: Numeic rating scale questionnaire.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactJahandide zahra

Shiraz University of Medical Sciences

nurs_midwif@sums.ac.ir+98 71 3647 4254

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 22, 2026