effect of pain management with self-care on pain and quality of life in patients with sickle cell disease

The effect of self-management of pain with self-care on nature of pain and quality of life in patients with sickle cell disease

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20160726029086N5

Enrollment

Registered

2020-04-15

Start date

2019-07-16

Completion date

Unknown

Last updated

2020-05-18

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

Conditions

Sickle Cell Disease.

Interventions

Intervention 1: Intervention group 1: The self-care group is a 25-person group that provides necessary education about self-care, such as nutrition, medication, and so on. Pain and quality of life que

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: The desire to participate in the study Be able to communicate in the context of transferring experiences Aged 18 years and up

Exclusion criteria

Exclusion criteria: Concurrent with complications from other chronic diseases Affected by any acute mental disorder and acute physical illness

Design outcomes

Primary

Measure	Time frame
Quality of life. Timepoint: Measurement of quality of life 1,2 and 3 months after intervention. Method of measurement: Quality of life questionnaire for sickle cell patients.;The Nature of Pain. Timepoint: Measuring the nature of pain 1, 2 and 3 months after the intervention. Method of measurement: McGill Pain Questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyyedeh Azadeh Moosapour

Ahvaz University of Medical Sciences

samoosapour@gmail.com+98 61 4377 4244

Outcome results

None listed

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