Effectiveness of Nurse Tele-consultation on the Quality of Elective Colonoscopy, Procedure-related Anxiety, and Financial Toxicity
Recruiting · NCT06887244 · Interventional (participants receive a specific treatment) · Lead sponsor: National Cancer Institute, Naples
View the official record on ClinicalTrials.gov →Interventions studied
Tele-consultation
What this trial is about
This is a multicenter, non-pharmacological, experimental, prospective, randomized study, with two arms (1:1) in a single-blind design. The study aims to evaluate the effectiveness of a tele-consultation procedure in patients undergoing elective colonoscopy in terms of quality of the exam, anxiety procedure-related and financial toxicity.
Who can take part
Age range
18 Years to 80 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Subjects eligible for outpatient pancolonoscopy:
- for diagnostic purposes;
- for screening purposes;
- for post-polypectomy follow-up;
- of both genders;
- of all ethnicities;
Exclusion criteria
- Patients under 18 years of age or over 80 years of age;
- Patients on waiting lists with SHORT priority: the procedure to be provided within a short time (no more than 10 days);
- Patients included in GOM pathways who undergo colonoscopy within 10 days;
- Pregnancy;
- Presence of known contraindications to bowel preparation;
- Presence of known contraindications to performing pancolonoscopy;
- Patients who have undergone colonic resection and/or have a colostomy/ileostomy;
- Patients with cognitive impairments;
- Patients declared legally incompetent or unable to understand and make decisions;
- Patients unable to provide informed consent.
Where it is running
1 location listed.
- S.S.D. Garoenterologia ed Endoscopia Digestiva - Naples, Italy