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The effect of self management program on elderly women with rheumatoid arthritis

Effectivness of "Chronic Disease Self-management Program" on reducing arthritis symptoms amongst elder women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015122425685N1
Enrollment
80
Registered
2016-02-01
Start date
2016-03-19
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. Seropositive rheumatoid arthritis-Other rheumatoid arthritis

Interventions

Intervention 1: The Intervention group: In this study the intervention will be holding the training sessions. Intervention 2: The control group: Training in control groups is not but after the end of
Behavior
The Intervention group: In this study the intervention will be holding the training sessions.

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
36 Years to 139 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria: Elderly people with rheumatoid arthritis that live in Tabriz and has a medical record at the Golgashte clinic. The exclusion criteria: Elderly people who are suffering from cognitive disorders, Elderly people who are not able to attending meetings according to diagnosed by specialists, Elderly people who diseases's pattern or manage will change during the project.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Self Management. Timepoint: Before the intervention and 1 month after interventio. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Self efficacy Skill. Timepoint: Before the intervention and 1 month after intervention. Method of measurement: Questionnaire.;Depression. Timepoint: Before the intervention and 1 month after intervention. Method of measurement: Questionnaire.;Mobility. Timepoint: Before the intervention and 1 month after intervention. Method of measurement: Questionnaire.;Compatibility with pain. Timepoint: Before the intervention and 1 month after intervention. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNayer Anvar

Tabriz University of Medical Sciences

majid.yousefi@ut.ac.iranvar.n60@gmail.comhm1349@gmail.com+98 41 3667 2380

Outcome results

None listed

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