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The effect of educational intervention on the quality of life promoting behaviors Patients with osteoporosis

The effect of educational intervention based on the Precede-Proceed Model on the quality of life promoting behaviors of female with osteoporosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241004063258N1
Enrollment
120
Registered
2024-11-03
Start date
2024-10-16
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

osteoporosis. Age-related osteoporosis without current pathological fracture

Interventions

Intervention 1: Intervention group: Receiving an educational program based on the PRECEDE-PROCEED model. Intervention 2: Control group: Not receiving any educational programs or interventions.

Sponsors

Rafsanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
30 Years to No maximum

Inclusion criteria

Inclusion criteria: Women with Osteoporosis: Diagnosis by the Treating Physician and Medical Records Minimum Literacy Requirement: Ability to Read and Write Absence of Mental Illness and Cognitive Disorders: No diagnosis of mental illnesses or cognitive disorders such as dementia and Alzheimer’s disease. No Autoimmune Diseases: Absence of autoimmune diseases, including rheumatoid arthritis. No Severe Illnesses: No severe conditions such as cancer, strokes, or heart attacks that impair daily functioning. No Recommended Physical Activity Limitations: No restrictions on physical activity advised by the treating physician.

Exclusion criteria

Exclusion criteria: Non-participation in Training Sessions: Absence from more than one training session. Diagnosis of New Acute Cardiovascular Diseases: Presence of new acute cardiovascular conditions. Lack of Willingness to Participate in the Study: Disinterest in joining the study. Occurrence of New Fractures: Development of new fractures.

Design outcomes

Primary

MeasureTime frame
Physical activity. Timepoint: 4 months after the intervention. Method of measurement: Physical Activity Questionnaire (IPAQ).;Calcium and vitamin D intake. Timepoint: 4 months after the intervention. Method of measurement: Food frequency questionnaire.

Secondary

MeasureTime frame
Quality of life. Timepoint: 4 months after the intervention. Method of measurement: Qualeffo-41 Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyedeh Shirin Lotfipur Rafsanjani

Rafsanjan University of Medical Sciences

lotfipur.shirin@gmail.com+98 34 3432 8214

Outcome results

None listed

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