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Clinical Trials in Turkey / NCT06757231
Active, not recruiting Not applicable

Chronic Care Model on Symptom Status, Stress and Quality of Life in Individuals With Inflammatory Bowel Disease

NCT06757231 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2024-02-13
Last updated
2025-01-03

Condition(s) studied

Inflammatory Bowel DiseasesColitis, UlcerativeCrohn Disease

Investigational drug(s) / intervention(s)

Nurse Counseling Based on the Chronic Care Model (CCM)

Nurse Counseling Based on the Chronic Care Model (CCM): This intervention involves personalized nurse counseling for patients diagnosed with Inflammatory Bowel Disease (IBD) based on the Chronic Care Model. The intervention includes: Biweekly phone consultations and weekly informational messages to provide education and support for symptom management, stress reduction, and quality-of-life improvement. An educational booklet to aid self-management. Follow-ups to assess progress, address concerns, and provide guidance on IBD management strategies.

Study summary

This study aims to evaluate the effects of nurse counseling provided based on the Chronic Care Model on symptom status, stress, and quality of life in individuals diagnosed with Inflammatory Bowel Disease (IBD).

Eligibility

Sex
ALL
Min age
12 Weeks
Max age
12 Weeks
Healthy volunteers
Accepted
Inclusion Criteria: * \- Individuals diagnosed with IBD who agree to participate in the study will be included after written informed consent form and informed consent form are obtained. * Have a confirmed diagnosis of IBD at least 6 months ago, * No obstacles to communication, * Can use a smartphone, * It will be determined from volunteers who agree to participate in the research on a voluntary basis. Exclusion Criteria: * \- IBHs for whom written consent cannot be obtained will be excluded from the study. * Those who wish to leave the research without completing the research with their own consent, * Patients who cannot have at least 3 interviews, * Patients who do not show up for the appointment for the final test will not be included.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Seval AKBEN Gaziantep Turkey (Türkiye)

More Hasan Kalyoncu University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06757231 on ClinicalTrials.gov ↗ ← All trials in Turkey