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Applying model on level of activity daily living and pain in arthritis rheumatoid patient.

Assessing the applying orem self-care model on level of activity daily living and pain in arthritis rheumatoid patient.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014052517840N1
Enrollment
60
Registered
2015-05-24
Start date
2013-08-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Rheumatoid arthritis. Rheumatoid arthritis, unspecified

Interventions

Intervention 1: Intervention group:Method in this study hold 4 training sessions in two system of supportive educative and partly compensatory system according to questionnaire for need assessment bas
before the intervention, second
one month after intervention and third
three months after intervention in test and control group.
Behavior
Intervention group:Method in this study hold 4 training sessions in two system of supportive educative and partly compensatory system according to questionnaire for need assessment based on Orem's Sel
Control group :This group did not receive any intervention and Just act according to their doctor's orders. Data from pain and activity daily living scale, were collected in three phases, first

Sponsors

Vice Chancellor for research of Tarbiat Modares University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:60 patients with moderate severity of rheumatoid arthritis in accordance with the American College of Rheumatology criteria which was confirmed by physician specialists and using the DAS28 for measuring the severity of rheumatoid arthritis;the aged range between 20-60;At least Literacy Exclusion criteria:In medical history, a history of cognitive problems such as dementia, psychosis, mental retardation? underlying diseases and disorders that are organic noticeable impact on performance.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: before the intervention, second; one month after intervention and third; three months after intervention. Method of measurement: Numeric pain scale.;Activities of daily living. Timepoint: before the intervention, second; one month after intervention and third; three months after intervention. Method of measurement: performance and satisfaction of Activities of daily living scale in Arthritis rheumatoid patient.

Secondary

MeasureTime frame
Stress, anxiety and depression. Timepoint: before the intervention, second; one month after intervention and third; three months after intervention. Method of measurement: DASS-21 scale.;Quality of life. Timepoint: before the intervention, second?; one month after intervention and third?; three months after intervention. Method of measurement: Quality of Life Questionnaire SF36.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElahe Sadat saeedifar

Tarbiat Modares university

elahe.saeedifar@modares.ac.ir+98 936 606 8600

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 6, 2026