The Effect of Telehealth Monitoring on Medication Compliance, Self-Efficacy and Quality of Life in Patients With İnflammatory Bowel Disease

Status: Recruiting
Location: See location...
Intervention Type: Other, Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This randomized controlled trial aims to evaluate the effect of nurse-led telehealth monitoring on medication adherence, self-efficacy, and quality of life in individuals with inflammatory bowel disease (IBD). The study will be conducted at the IBD Outpatient Clinic of Istanbul University-Cerrahpaşa, Cerrahpaşa Medical Faculty. Participants will be randomly assigned to either an intervention group receiving a 3-month structured telehealth program (including education, counseling, phone calls, and reminders) or a control group receiving only standard care and an educational booklet. Outcomes will be assessed at baseline and after 12 weeks.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Individuals aged 18 years or older

• Able to read and write in Turkish

• Diagnosed with inflammatory bowel disease (IBD) for at least 6 months

• In clinical remission (Harvey-Bradshaw Index score \< 5 or Simple Clinical Colitis Activity Index score \< 3)

• Able to use a smartphone

• Have access to an online messaging application (e.g., WhatsApp) and a valid e-mail address

• Capable of downloading and using a mobile or computer-based video conferencing application (e.g., Zoom)

• Willing to participate in the study voluntarily

Locations
Other Locations
Turkey
Istanbul University - Cerrahpasa Cerrahpaşa Faculty of Medicine Department of Gastroenterology
RECRUITING
Istanbul
Contact Information
Primary
Kimya Kılıçaslan, PhD Candidate
kimya.kilicaslan@iuc.edu.tr
+90 535 083 45 53
Backup
Zeliha Tulek, PhD, Prof.
ztulek@iuc.edu.tr
+90 532 776 29 93
Time Frame
Start Date: 2024-04-20
Estimated Completion Date: 2025-05-30
Participants
Target number of participants: 120
Treatments
Experimental: Intervention Group
Participants in the intervention group will be included in a structured telehealth monitoring program led by a nurse for 12 weeks.
Other: Control group
Participants in the control group will only receive standard care. No additional interventions will be implemented during the 12-week period.
Related Therapeutic Areas
Sponsors
Leads: Istanbul University - Cerrahpasa

This content was sourced from clinicaltrials.gov