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Physical and Psychological Profiles Associated With Patient's Preference for ESRD Treatment

C

Centre Hospitalier Universitaire de Nice

Status

Completed

Conditions

End Stage Renal Failure

Treatments

Other: Evaluation of psychological phenotype

Study type

Interventional

Funder types

Other

Identifiers

NCT01834755
12-AOI-03

Details and patient eligibility

About

Highlighting the relationship between psychological and physical profiles and patient's preference to better understand the patient's treatment preference and improve the information provided.

Full description

CKD is a Public Health Problem with a prevalence of 10% in general population. For patients reaching The making decision to treat ESRD with renal replacement therapy is a complex process and needs to be shared between patients, family, physician and nephrologist.

Systematic Information delivery about several treatments of ESRD is recommended for patients and his family (Hemodialysis, Peritoneal Dialysis, Kidney Transplantation and Conservative treatment). Some studies on the preference of patients for renal replacement therapy reported a choice for PD about 50% while the registers report a low diffusion of PD (around 10%). Since 2009 we propose a systematic information about the different therapeutic options for ESRD and identified some clinical characteristics associated to patient's preference. However we want to know if psychological or physical phenotype is associated to patient's preference.

The objective of the study is to highlight the relationship between psychological and physical profiles and patient's preference to better understand the patient's treatment preference and improve the information provided.

Enrollment

60 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • More than 18 years
  • CKD with estimated GFR below 20 ml/min/1.73m2 without dialysis treatment
  • Patient who accepts information delivery about treatments of ESRF
  • Patient who accepted and signed the informed consent
  • Subject beneficiary of a social security system

Exclusion criteria

  • Inability to achieve psychological tests
  • Inability to achieve physical tests

Trial design

Primary purpose

Health Services Research

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

60 participants in 1 patient group

single arm
Other group
Description:
Evaluation of psychological phenotype with several questionnaire (Big Five, EPADV-16), physical activity with a self-administered questionnaire (Baecke) and several test ( SPPB, Handgrip Strengh test, MicroFET 2 Digital Dynamometer)
Treatment:
Other: Evaluation of psychological phenotype

Trial contacts and locations

1

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Central trial contact

Olivier MORANNE, MD

Data sourced from clinicaltrials.gov

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