Trial on Education And Clinical Outcomes for Home PD Patients (TEACH)

Kook-Hwan Oh

Status

Completed

Conditions

Risk Reduction

Treatments

Behavioral: Intensive training group

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT01204619

TEACH

Details and patient eligibility

About

Since the emergence of home peritoneal dialysis as an alternative to in-center hemodialysis for chronic renal replacement therapy in the late 1970s, the percentage of dialysis patients on PD has continued to decrease each year. There have been a growing concern and research on patient and technique survival of peritoneal dialysis versus hemodialysis to find influential factors for better clinical outcomes. Meanwhile, technique failure rates were significantly higher in small centers treating less than twenty five PD patients. And there was a result for better technique survival after the second year, among the patients trained at the BREC(Baxter Renal Education Center). Better technique survival in large centers can be assumed with not only their more experience with patient management but also their educational infrastructure compared to small-sized centers.

Throughout our experiences in the last 30 years, we have recognized that a major element of PD program is patient training, however few data are available in terms of the relationship between PD training and treatment outcome and mostly are retrospective and non-randomized. Moreover, the technique survival and patient survival were analyzed with no significant difference.

From the insight, we decided to study prospectively to evaluate the efficacy of well-structured education program in terms of various patient outcomes in incident patients on PD.

Full description

This study will be conducted as multi-center, open-label, randomized, controlled trial. One hundred four patient starting PD will be randomized into two training groups. Patients in the conventional training group (CG) will be given non-standardized in-center conventional training programs plus two sessions of training by home visit, while those in intensive training group (IG) given in-center conventional training programs plus repeated home visits regularly over 24-month period (total thirteen visits). The primary end point of the study is exit site infection (ESI). Secondary endpoints are peritonitis and all-cause infection. Generalized Estimating Equations will be used to assess the adjusted effect of training level on the ESI and Cox regression model employed to evaluate the effect on the peritonitis and other secondary outcomes.

Enrollment

104 patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Incident patients who have PD catheter insertion for starting PD with Baxter solutions
> 20 yr of age

Exclusion criteria

Patients who have undergone dialysis or received kidney transplant (note, however, that patients who are currently undergoing emergency hemodialysis temporarily right before the PD do not fall under the exclusion criteria.)
Patients who are likely to receive kidney transplant or shift to hemodialysis within the following 1 year
Patients diagnosed with acute inflammatory disease for the past three months
Patients currently diagnosed with chronic inflammatory disease
Currently pregnant or breastfeeding
Patients who are involved in other clinical trial within 30 days prior to enrollment
Patients who are currently hospitalized in care facilities such as nursing home, etc., or those who are expected to be hospitalized for the duration of the clinical test
Patients who cannot perform PD by themselves
Patients considered by the person in charge of the clinical test to have difficulty in participating in this clinical test