Quality of Life Clinical Trial
Official title:
The Effect of Web-Based Patient Education on Quality of Life of Patients With Colostomy and Ileostomy: A Randomized Controlled Trial
The purpose of the study is to develop, implement and determine the effects of web-based education programs for patients undergoing colostomy and ileostomy.The study is a randomized controlled experimental research with a pre-test post-test control group design. The study group of the research consisted of individuals, who have an abdominal stoma procedure at a Training and Research Hospital operating under the Ministry of Health in Turkey. 35 individuals were enrolled to the experiment and control groups (N=70). The study group of the hospital was determined as a result of the power analysis performed on an average number of 150 patients, on whom a stoma is opened within a year, with an estimated effect rate of 0.824 and a SD of 0.45, the power being 0.80 and confidence interval p:0.05, as a total of 50 patients, 25 in the experiment group and 25 in the control group. Taking into consideration the data loss that may be experienced, it was planned to enrol 35 individuals to the experiment group and 35 individuals to the control group. The patients were randomly assigned to each group. Homogeneity of patients randomized to the experiment and control groups was checked with a t-test. Research data were collected using an Information Form, Stoma Complications Assessment Form and City of Hope-Quality of Life-Ostomy Questionnaire and Stoma Care Knowledge Assessment Test.
The purpose of the study is to develop, implement and determine the effects of web-based
education programs for patients undergoing colostomy and ileostomy.
The study is a randomized controlled experimental research with a pre-test post-test control
group design. The study group of the research consisted of individuals, who have an abdominal
stoma procedure at a Training and Research Hospital operating under the Ministry of Health in
Turkey. 35 individuals were enrolled to the experiment and control groups (N=70). The study
group of the hospital was determined as a result of the power analysis performed on an
average number of 150 patients, on whom a stoma is opened within a year, with an estimated
effect rate of 0.824 and a SD of 0.45, the power being 0.80 and confidence interval p:0.05,
as a total of 50 patients, 25 in the experiment group and 25 in the control group. Taking
into consideration the data loss that may be experienced, it was planned to enrol 35
individuals to the experiment group and 35 individuals to the control group. The patients
were randomly assigned to each group. Homogeneity of patients randomized to the experiment
and control groups was checked with a t-test. The stages of the research design were
determined completely in accordance with the CONSORT diagram. Data were collected using an
Information Form, Stoma Complications Assessment Form and City of Hope-Quality of Life-Ostomy
Questionnaire and Stoma Care Knowledge Assessment Test. The study data were analysed with
average, standard deviation, frequency, student t test, paired sample t test, variance
analysis, Fisher's exact chi-square test, Fisher-Freeman-Halton test and Yates continuity
correction test. Significance was assessed at a level of p<0.05.
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