the Effect of the Interactive Nurse Support Program, Developed as a Mobile Application, on Patient Outcomes in Colorectal Cancer Patients Receiving Chemotherapy During the Covid-19 Process

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

The aim of this study is to determine the effect of the interactive nurse support program developed as a mobile application on patient outcomes (symptom management, quality of life, perception of social support and anxiety) in colorectal cancer patients receiving chemotherapy during the COVID-19 process; It was planned in a randomized controlled, single-blind design. In the study, a mobile application will be designed for colorectal cancer patients with the content created in line with the literature. In the application, the about COVID-19 module, which includes information for colorectal cancer patients during the COVID-19 process, the learning module in which the symptoms and suggestions for colorectal cancer patients receiving chemotherapy are included, the discussion module where patients can share their knowledge and experiences with each other, The ask the expert module, where nurses and physicians can ask questions, will be comprised of the lived stories module and the communication sections, which include interview videos made with individuals who are in remission only after completing the treatment related to the disease. A pretest consisting of Personal Information Form, Multidimensional Perceived Social Support Scale EORTC QLQ-C30 and CR29 Quality of Life Scale, ECOG Performance Scale and Beck Anxiety Scale will be administered to all patients included in the study. The mobile application will be installed on the phones of the patients in the experimental group and they will be used for 12 weeks. Patients in the control group will receive standard care during this process and no intervention will be made. In the sixth and twelve weeks, all participants will be given a posttest. The change in symptom management, quality of life, perceived social support and anxiety levels of the experimental group after mobile application use will be evaluated.

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

• Volunteering to participate in research

• Be over 18 years old

• Being diagnosed with stage 0.1,2 colorectal cancer

• Ability to understand and speak Turkish

• ECOG performance score of 0.1 or 2

• Being literate

• Having a mobile phone with an Android processor and being able to use it effectively

• First time receiving chemotherapy

Locations
Other Locations
Turkey
Ankara Bilkent City Hospital
RECRUITING
Ankara
Contact Information
Primary
burcu ağdemir, res. assis.
bagdemir@ankara.edu.tr
+90 531 402 62 56
Backup
ayten demir, professor
aytendemir@ankara.edu.tr
+90 532 549 79 27
Time Frame
Start Date: 2022-07-15
Estimated Completion Date: 2024-04-28
Participants
Target number of participants: 100
Treatments
Experimental: experimental group
As an intervention, the mobile application called KRK-İnHED will be installed on the patients' phones. Patients in the experimental group will be interviewed the day before chemotherapy starts.~Personal Information Form, Multidimensional Perceived Social Support Scale, Quality of Life Scale, Beck Anxiety Scale will be filled in these patients.~Mobile application will be installed on the patient's phone by the researcher. The patient will be registered to the program by creating a user name.~The patient will be given 15-20 minutes of online training on the use of the mobile application.~The mobile application will be applied for a total of 12 weeks for 4 cycles (1 cycle/3 weeks) from the first day of chemotherapy treatment.
No_intervention: control group
Patients in the control group who will not have a mobile application installed on their phones will receive standard care.
Related Therapeutic Areas
Sponsors
Leads: Ankara University

This content was sourced from clinicaltrials.gov