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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05796544
Other study ID # N.119.22
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 14, 2023
Est. completion date April 1, 2025

Study information

Verified date September 2023
Source University of Rome Tor Vergata
Contact Ercole Vellone, Professor
Phone +390672596871
Email ercole.vellone@uniroma2.it
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary aim of this study is to evaluate whether remote education is as effective as in-person education in improving self-care behaviors of ostomy patients.


Description:

After signing the informed consent form, patients with ostomy will be assigned to the intervention or active control group (1:1). The intervention group will receive a total of four remote educational sessions over 2 months. The control group will receive the standard care, consisting of in-person standard education.


Recruitment information / eligibility

Status Recruiting
Enrollment 384
Est. completion date April 1, 2025
Est. primary completion date December 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 120 Years
Eligibility Inclusion Criteria: 1. having undergone a surgical operation with subsequent ostomy placement; 2. being at least 18 years old of age; 3. absence of cognitive decline, 4. absence of any 5. being able to manage the software on the smartphone 6. be willing to participate to the trial and sign the informed consent form. Exclusion Criteria: 1. presence of a cognitive decline, assessed with a score > 4 at the Six-item Screener 2. presence of any stomal or peristomal complication 3. not being able to read and speak Italian language

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Remote self-care education
The intervention group will receive a total of four remote educational sessions over 2 months.
In-person self-care education
The active comparator group will receive a total of four in-person educational sessions over 2 months.

Locations

Country Name City State
Italy Azienda SS. Antonio e Biagio e Cesare Arrigo - Alessandria
Italy Istituto Tumori Pascale Napoli Napoli
Italy Arcispedale S. Maria Nuova Azienda ospedaliera di Reggio Emilia Reggio Emilia
Italy Ambulatorio infermieristico per pazienti stomizzati ASL Roma2 S.Eugenio Pertini Roma Rome
Italy Tor Vergata Hospital Roma

Sponsors (1)

Lead Sponsor Collaborator
University of Rome Tor Vergata

Country where clinical trial is conducted

Italy, 

References & Publications (3)

2. Villa, G., Vellone, E., Sciara, S., Stievano, A., Proietti, M. G., Manara, D. F., ... & Pantaleo, G. (2019). Two new tools for self-care in ostomy patients and their informal caregivers: Psychosocial, clinical, and operative aspects. International Journal of Urological Nursing, 13(1), 23-30.

Costa, A., Maria, M., Campos, C., & Santos, J. D. (2020). Effect of educational intervention in postoperative people with intestinal elimination stomies: systematic review. doi:10.6018/eglobal.19.1.368501

Riegel B, Jaarsma T, Stromberg A. A middle-range theory of self-care of chronic illness. ANS Adv Nurs Sci. 2012 Jul-Sep;35(3):194-204. doi: 10.1097/ANS.0b013e318261b1ba. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Self-care maintenance Self-care maintenance will be measured with the Ostomy Self-care Index (OSCI). Scores range from 0 to 100, with higher scores indicating better self-care maintenance 1 month after the last intervention
Secondary Self-care monitoring Self-care monitoring will be measured with the Ostomy Self-care Index (OSCI). Scores range from 0 to 100, with higher scores indicating better self-care monitoring 1 month after the last intervention
Secondary Self-care management Self-care management will be measured with the Ostomy Self-care Index (OSCI). Scores range from 0 to 100, with higher scores indicating better self-care management 1 month after the last intervention
Secondary Self-care self-efficacy Self-care self-efficacy will be measured with the Ostomy Self-care Index (OSCI). Scores range from 0 to 100, with higher scores indicating better self-care self-efficacy 1 month after the last intervention
Secondary Stoma-specific quality of life Stoma-specific quality of life will be measured with the Stoma Specific Quality of Life Index- Scores on this scale range from 20 to 80, with higher scores meaning higher quality of life 1 month after the last intervention
Secondary Depression Depression will be measured with the Patient Health Questionnaire 9 (PHQ-9). Scores on this scale range from 0 to 27, with higher scores indicating higher depression 1 month after the last intervention
Secondary Adjustment to the stoma Adjustment to the stoma will be measured with the Stoma Adjustment Inventory-23. scores on this scale range from 0 to 92, with higher scores meaning better adjustment 1 month after the last intervention
Secondary Stomal and peristomal complications rates Stomal and peristomal complications rates will be collected with a questionnaire developed by the research team. 1 month after the last intervention
Secondary Health care service utilization Health care service utilization will be collected with a questionnaire developed by the research team. 1 month after the last intervention
Secondary Mobility (distance in km from the patient house to the hospital and vice versa, means of transportation used, and presence of a companion) Mobility will be collected with a questionnaire developed by the research team. 1 month after the last intervention
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