End-stage Renal Disease Clinical Trial
Official title:
Improving Patient-clinician Communication Among End-stage Renal Disease African Patients and Their Families
| Verified date | March 2008 |
| Source | University of Pittsburgh |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The specific aims are:
1. to evaluate the feasibility and acceptability of PC-ACP among African American patients
with End-stage Renal Disease and their surrogates and
2. to examine preliminary effects of PC-ACP on patient and surrogate outcomes (patients'
perceived quality of communication, surrogates' level of comfort in decision making for
the patient, patients' difficulty in making choices, patient-surrogate congruence in
goals of care, and patients' and surrogates' psychosocial/spiritual receptiveness) at
one week following receipt of the intervention.
| Status | Completed |
| Enrollment | 42 |
| Est. completion date | December 2008 |
| Est. primary completion date | June 2007 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: 1. have been on either center-hemodialysis or home-peritoneal dialysis 2. are cognitively intact,i.e., able to communicate, able to understand information, able to make choices and give rationale, 3. have an individual who can be present during the intervention as a surrogate decision maker, 4. are over 18 years of age, and 5. are able to communicate in English. Surrogates must be over 18 years of age and be able to communicate in English. |
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| University of Pittsburgh |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | congruence between patient and surrogate at one week after intervention | one week post intervention | ||
| Primary | patient and surrogate satisfaction with communication | one week post intervention |
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