- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00428012
Quality of Life Therapy for Adults With ESRD Awaiting Renal Transplantation
5. januar 2012 opdateret af: James Rodrigue, Beth Israel Deaconess Medical Center
The purpose of this study is to determine whether psychological intervention is effective in improving quality of life, mood, and relationships among adults with end-stage renal disease who are awaiting kidney transplantation.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Despite known quality of life (QOL) deficits associated with end-stage renal disease (ESRD), there have been very few attempts to develop strategies to improve QOL in adults with ESRD awaiting renal transplantation.
The long-term goal of this research program is to better understand how QOL can be enhanced, to identify the mechanisms underlying QOL changes, to identify which patients benefit most from QOL intervention, and to determine whether QOL benefits can extend beyond transplantation.
The objective of this research is to determine the effectiveness, feasibility and applicability of Quality of Life Therapy (QOLT) in treating adults with ESRD awaiting renal transplantation.
In a recent small, single-center clinical trial, we demonstrated that QOLT can improve QOL, psychological functioning, and social intimacy in patients awaiting lung transplantation.
We now seek to examine whether this intervention can be effectively adapted and implemented with adults with ESRD who are awaiting renal transplantation.
The central hypothesis is that by targeting improvements in specific life domains, QOLT yields significant clinical benefits in QOL, psychological functioning, and the patient-caregiver relationship.
This hypothesis is being tested by pursuing three specific aims: 1) Determine the effectiveness of QOLT; 2) Examine the differential effectiveness of QOLT by race (White, African American); and 3) Assess the feasibility of a multisite R01 application.
Under the first aim, adults with ESRD awaiting renal transplantation are being randomized to receive QOLT, Supportive Therapy (ST), or Standard Care (SC).
Primary outcomes are changes in QOL, psychological functioning, and social intimacy at 1 and 12 weeks post-treatment.
Under the second aim, the relationship between race and intervention outcomes will be closely examined.
Under the third aim, attrition rates, reasons for attrition, therapist adherence to treatment protocols, and participant satisfaction ratings are being gathered to assess the need for protocol changes prior to developing a larger, multisite clinical trial R01 application.
This study is innovative because it is among the first to evaluate a theoretically-driven psychological intervention to specifically improve QOL in the context of ESRD and renal transplantation.
The research is significant because it is expected to advance and expand understanding of how QOL can be improved in patients with ESRD.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
65
Fase
- Fase 2
- Fase 3
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Massachusetts
-
Boston, Massachusetts, Forenede Stater, 02215
- The Transplant Center, Beth Israel Deaconess Medical Center
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
21 år til 70 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Male or female patients between 21 and 70 years of age
- Diagnosis of ESRD
- Wait-listed for deceased donor renal transplantation (primary transplant only)
- White or African American race
- Signed informed consent
- Primary caregiver identified as spouse or domestic partner
- Resides within 60 minutes of transplant center
Exclusion Criteria:
- Prior recipient of renal transplantation
- Prior recipient of other solid organ transplantation
- Wait-listed for combined kidney-pancreas transplantation
- Current substance abuse or dependency
- Currently hospitalized
- Current recipient of psychological intervention services
- Mental retardation
- Substantial cognitive impairment (score of 23 or less on the Mini-Mental State Examination)
- Communication difficulties (speech, hearing) so substantial that they would prevent patient from participating actively in one of the interventions (determined by transplant social worker)
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Ingen indgriben: Standardpleje
|
|
|
Eksperimentel: QOLT
Quality of Life Therapy (QOLT) 8 weekly individual counseling sessions
|
8 weekly individual counseling sessions
|
|
Aktiv komparator: ST
Supportive Therapy (ST) 8 weekly individual counseling sessions
|
8 weekly individual counseling sessions
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Primary: Scores on the following measures at 12 weeks post-intervention: Quality of Life Inventory, SF-36, KDQoL, CDC Activity Limitations Module, Hopkins Symptom Checklist, POMS, and Miller Social Intimacy Scale
Tidsramme: 12 weeks
|
12 weeks
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: James R. Rodrigue, PhD, Beth Israel Deaconess Medical Center
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. januar 2007
Primær færdiggørelse (Faktiske)
1. juli 2009
Studieafslutning (Faktiske)
1. april 2011
Datoer for studieregistrering
Først indsendt
25. januar 2007
Først indsendt, der opfyldte QC-kriterier
25. januar 2007
Først opslået (Skøn)
29. januar 2007
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
6. januar 2012
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
5. januar 2012
Sidst verificeret
1. januar 2012
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- R21 DK77322 (completed)
- R21DK077322 (U.S. NIH-bevilling/kontrakt)
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Slutstadie nyresygdom
-
Uppsala UniversityUppsala University HospitalIkke rekrutterer endnuMR | Anæstesi | Renal blodgennemstrømning | Renal iltning
-
Universitaire Ziekenhuizen KU LeuvenAfsluttetForekomst af Augmented Renal Clearance | Risikofaktorer for øget renal clearanceBelgien
-
Medical University of ViennaAfsluttetGlomerulær filtreringshastighed | Fedtsyrer, ikke-esterificerede | Renal Cirkulation | Renal Plasma FlowØstrig
-
The First People's Hospital of ChangzhouIkke rekrutterer endnu
-
Andrew B AdamsBristol-Myers SquibbAfsluttet
-
Hospices Civils de LyonAfsluttetSkadelig virkning | Renal toksicitetFrankrig
-
University Health Network, TorontoAfsluttetGlomerulær filtreringshastighed | Renal blodgennemstrømningCanada
-
National Cancer Institute (NCI)AfsluttetLunge | Bryst | Ovarie | Cervikal | RenalForenede Stater
-
Oregon Health and Science UniversityAfsluttet- Undersøgelsesfokus: Renal retention af lipidmikroboblerForenede Stater
Kliniske forsøg med Quality of Life Therapy
-
Seoul National University HospitalTrukket tilbageDepression | Postoperative komplikationer | Angst | MestringsadfærdKorea, Republikken
-
Memorial Sloan Kettering Cancer CenterAfsluttetAscitesForenede Stater
-
Latin American Cooperative Oncology GroupRoche Pharma AG; EVA - Grupo Brasileiro de Tumores GinecológicosAfsluttet
-
Ankara UniversityAfsluttetStørre abdominal kirurgi | Patientrapporteret resultatKalkun
-
University of FloridaAfsluttet
-
World Vision CanadaRyerson University; World Health Organization; Global Affairs Canada; Ministry...AfsluttetDiarré | Malaria | Akut luftvejsinfektion
-
University Hospital, Strasbourg, FranceAfsluttetKirurgisk indgreb | MindreFrankrig
-
King's College LondonGuy's and St Thomas' NHS Foundation TrustAfsluttet
-
Beijing Tsinghua Chang Gung HospitalRekrutteringPostoperative komplikationer | Cerebrovaskulær ulykke | Større uønskede hjertehændelser | ModellerKina
-
Ondokuz Mayıs UniversitySamsun Education and Research HospitalAfsluttet