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The effect of interaction education on patients with celiac disease

Study the effect of interactive education on adherence to diet ,quality of life and functional indicators in patients with celiac disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170926036426N4
Enrollment
30
Registered
2019-04-09
Start date
2018-09-09
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

Celiac.

Interventions

Intervention 1: Intervention group:Providing interactive education on the diet of patients with celiac disease who provided this training for four sessions of 90 minutes over a period of four weeks in

Sponsors

Zahedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Celiac disease, the diagnosis of celiac disease, is documented by a specialist in the medical records of the patient no chronic disease (e.g., diabetes), hypothyroidism, hyperthyroidism no mental disorders no problem in communication (e.g., blindness or deafness) non-pregnant women above 18 years old

Exclusion criteria

Exclusion criteria: special and incurable diseases inability to learn

Design outcomes

Primary

MeasureTime frame
Compliance with a gluten-free diet. Timepoint: Before the intervention and 4 weeks after providing interactive education. Method of measurement: Dietary compliance questionnaire.;Quality of Life. Timepoint: Before the intervention and 4 weeks after providing interactive education. Method of measurement: Quality of life questionnaire for patients with celiac disease.;Serum iron. Timepoint: Measurement of serum iron before intervention and four months after intervention. Method of measurement: Perform a test with a fully automatic B.T 3000 machine.;Serum vitamin D. Timepoint: Measurement of serum vitamin D before intervention and four months after intervention. Method of measurement: Performing the experiment with FOMO ELITE ARIDER.;Body mass index. Timepoint: Measurement of height and weight before intervention and four months after intervention. Method of measurement: Height and weight measurements with HBMI PLUS-CR device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFateme Gharebaghi

Zahedan University of Medical Sciences

f.gharebaghi@yahoo.com+98 54 3344 2481

Outcome results

None listed

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