1. Participation in an early home-based education programme compared to care as usual will significantly increase knowledge on kidney disease and treatment options, communication on renal replacement options and promote a positive attitude towards…
ID
Bron
Aandoening
Kidney disease
Kidney failure
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Patients:<br>
1. Attitude towards renal replacement therapy: T0, T1, T2;<br>
2. Attitude towards communication on renal replacement therapy: T0, T1, T2;<br>
3. Communication about renal replacement therapy: T0, T1, T2;<br>
4. Knowledge about renal replacement therapy: T0, T1, T2;<br>
5. Subjective norm: T0, T1, T2;<br>
6. Perception of control: T0, T1, T2;<br>
7. Anticipated regret: T0, T1, T2;<br>
8. Selfidentity: T0, T1, T2;<br>
9. Intention to communicate about renal replacement therapy options. T0, T1, T2;<br>
10. Moral norm: T0, T1, T2.
<br><br>
Social network (family and friends of the patient):<br>
1. Attitude towards communication on renal replacement therapy: T0, T1;<br>
2. Attitude towards living donation: T0, T1;<br>
3. Communication about renal replacement therapy: T0, T1;<br>
4. Knowledge about renal replacement therapy: T0, T1;<br>
5. Subjective norm: T0, T1;<br>
6. Perception of control: T0, T1;<br>
7. Anticipated regret: T0, T1;<br>
8. Selfidentity: T0, T1;<br>
9. Intention to communicate about renal replacement therapy options. T0, T1.
Achtergrond van het onderzoek
Transplantation with the kidney from a living donor has significant advantages for patient and transplant survival when compared to transplantation with a kidney from a deceased donor. Moreover, patient and transplant survival is most optimal when dialysis can be completely avoided. However, a large proportion of patients first start dialysis before they are transplanted with a kidney from a living donor. The main aim of this study is to develop an intervention to change knowledge, communication and attitudes regarding renal replacement therapy (RRT). The second aim is to investigate whether this intervention has an impact on the proportion of patients undergoing haemodialysis, peritoneal dialysis or transplantation as their first form of RRT.
This is a prospective randomised cross-over study. Patients with a MDRD of 25 ml/min for whom there is an indication for RRT within 1 or 2 years are included. Family and friends of these patients will also be invited to participate.
The intervention consists of a first intake consultation and a home-based educational meeting. The patient invites their family and friends to attend the house-call educational meeting. During this meeting the social worker will discuss the kidney, kidney disease, possible treatment options, and the consequences for quality of life. There will be the possibility to ask questions and to discuss these topics. Written information (leaflets) will be left behind after the meeting. The educational meetings will be carried out by trained medical social workers in 4 hospitals in the Rotterdam area.
Primary study outcome of the study: Change in knowledge, attitude, and communication about RRT among both the patient and their family and friends.
Secundary study outcome of the study: The proportion of patients who undergo haemodialysis, peritoneal dialysis or pre-emptive transplantation as their first form of RRT.
Doel van het onderzoek
1. Participation in an early home-based education programme compared to care as usual will significantly increase knowledge on kidney disease and treatment options, communication on renal replacement options and promote a positive attitude towards transplantation compared to dialysis;
2. Participation in the early home-based education programme will be related to greater likelihood of undergoing a pre-emptive renal transplantation.
Onderzoeksopzet
Patients: T0, T1, T2.
At baseline all patients will complete the questionnaire during the first consultation. Between T0 and T1 Group 1 will receive the intervention while Group 2 receives care-as-usual. At T1 (4 weeks later) all patients complete the same questionnaire. Between T1 and T2, Group 1 will receive care-as-usual while Group 2 receives the intervention. All patients will complete the questionniare at T2 (4 weeks after T1).
Social network: T0, T1.
All family and friends of the patient who are invited to attend the educational meeting will receive an invitation along with the T0 questionnaire. T1 will be handed out after the educational meeting to be completed within one week.
Onderzoeksproduct en/of interventie
An early education programme (consisting of an introductory session and a group education session for patient and their social network in the home of the patient) versus care as usual (regular patient education in the hospital and care from the treating nephrologist).
Publiek
Postbus 2040
E.K. Massey
Rotterdam 3000 CA
The Netherlands
+31 (0)10 7033451
e.massey@erasmusmc.nl
Wetenschappelijk
Postbus 2040
E.K. Massey
Rotterdam 3000 CA
The Netherlands
+31 (0)10 7033451
e.massey@erasmusmc.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. Patients for which there is a medical indication for renal replacement therapy within 1 to 2 years (25 MDRD ml/min taking into account the rate of progression);
2. Patients > 18 years;
3. Family and friends of the patient > 18 years of age.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Patients or family/friends who are unable to read or speak the Dutch language sufficiently.
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL2605 |
NTR-old | NTR2733 |
Ander register | Nierstichting : SB115 |
ISRCTN | ISRCTN wordt niet meer aangevraagd. |