search
Back to results

Effect on Pre-operative Anxiety of a Personalized Three-dimensional Kidney Model Prior to Nephron-sparing Surgery- Rein 3D Anxiety (R3DP-A)

Primary Purpose

Tumoral Kidney

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
3D model pré-operative education
Sponsored by
University Hospital, Bordeaux
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Tumoral Kidney focused on measuring Kidney Neoplasms, Renal-Cell Carcinoma, Nephron-Sparing Surgery, 3D Modeling, 3D Printing, Anxiety, STAI, Personalized Medicine

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Adult patients (≥ 18 years of age) Scheduled surgical management by laparoscopic partial nephrectomy with robotic assistance for kidney tumor Unilateral kidney tumor or 1st surgery for bilateral involvement Consent expressed for integration of the UroCCR cohort, Expressed consent for participation in the 3D Anxiety study. Patients affiliated or benefiting from a social security plan Exclusion Criteria: Refusal of consent or participation Difficulty understanding and expressing oneself in French Patient under guardianship or curatorship No preoperative CT scan available for 3D modeling

Sites / Locations

  • CHU d'ANGERSRecruiting
  • CHU de BordeauxRecruiting
  • CHU de CAENRecruiting
  • Hôpital Kremlin-Bicêtre
  • CHU de La CONCEPTION
  • CHU de NANTES

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

No Intervention

Arm Label

Virtual 3D model group

3D Printed Model Group

Control group

Arm Description

exchange time with the virtual 3D model of the kidney to be operated on as information support

eexchange time with the printed three-dimensional model of the kidney to be operated on as information support

discussion time with the patient information sheet of the French Association of Urology (AFU) as information support

Outcomes

Primary Outcome Measures

Measurement of the mean pre-operative anxiety score per arm, by filling the STAI-state self-questionnaire
The STAI-Etat will be collected before surgery to evaluate the effect of using a personalized three-dimensional model of the patient's kidney during a pre-operative information visit .

Secondary Outcome Measures

Measurement of the progression of the mean anxiety score per arm, by filling STAI-Trait Anxiety self-questionnaire.
The progression of the mean anxiety score per arm, measured by STAI-State self-questionnaire at the three follow-up visits in the study and adjusted on the STAI-Trait score at baseline will assess feelings of apprehension, tension, nervousness and worries that the subject usually feels.
Measurement of the progression in mean health literacy questionnaire score HLSEU-Q16 between baseline and 15-day post-operative follow-up per arm
This questionnaire is a short version version of the European Health Literacy Survey Questionnaire based on a model including 4 health information processing skills: accessing, understanding, evaluating and applying application of health information .
Measurement of the mean pre-operative score for understanding disease and choice of treatment per arm by filling the WAKE questionnaire
The WAKE questionnaire is used assess the feeling of understanding of the disease and the choice of treatment preoperatively in each of the three groups, the questionnaire comprises five question on the understanding of the disease . Each dimension has 5 levels : very poor, poor,faire, good, very good or strongly desagree, disagree,neutral,agree or strongly agree
Measurement of the progression of quality of life in each of the three groups by filling the EQ-5D-5L questionnaire
The EQ-5D-5L questionnaire measures participants' quality of life.The descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. Additinonally, the questionnaire records the patient's self-rated health on a vertical visual analogue scale, where the endpoints are labelled 'The best health you can imagine' and 'The worst health you can imagine'.
Measurement of the average duration of the pre-operative information visit in each of the three groups

Full Information

First Posted
August 28, 2023
Last Updated
October 13, 2023
Sponsor
University Hospital, Bordeaux
search

1. Study Identification

Unique Protocol Identification Number
NCT06035211
Brief Title
Effect on Pre-operative Anxiety of a Personalized Three-dimensional Kidney Model Prior to Nephron-sparing Surgery- Rein 3D Anxiety
Acronym
R3DP-A
Official Title
Effect on Pre-operative Anxiety of a Personalized Three-dimensional Kidney Model Prior to Nephron-sparing Surgery for Renal Tumor. R3DP-A
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 19, 2023 (Actual)
Primary Completion Date
September 2025 (Anticipated)
Study Completion Date
January 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Bordeaux

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this clinical trial is to evaluate the impact of showing and handling a three-dimensional modelization of a patient's tumoral kidney the day before his nephron-sparing surgery. The main outcome measure was the effect on anxiety assessed via the STAI state score. 3 types of pre-operative information were compared (3D virtual model, 3D printed model, and information) using a randomization.
Detailed Description
Announcement of serious illnesses and especially cancerous disease has major impacts on one's psychological field. Need of surgery can create even other fears due to its unknown nature. Use of tools to decrease anxiety and enhance understanding prior to surgery is a key point in comprehensive care that is way not enough promoted for now. In the field of surgery, available methods to deal with pre-operative anxiety are massively represented by anxiolytics drugs, only few other devices were evaluated. Technological development in healthcare has seen the rising of three-dimensional media, especially in surgery, for procedure planning. There is no doubt that this tool is effective in helping surgeons regarding the studies published within the past few years but there is no such evidence concerning the benefit for patients. Some authors report improvement of patients understanding and great satisfaction referring to the usefulness of this tool. But none of these papers evaluated anxiety. The goal of this research is to measure the effect of a personalized three-dimensional model of patients' tumoral kidney on peri-operative anxiety. For this purpose this clinical trial is designed as following: a total of 234 (78*3) patients planned to have a nephron-sparing surgery for kidney tumor are going to be randomly assign in 3 different groups. Inside the 2 interventional groups, patients' kidneys will be modelled in three dimensions, but in one of the two groups, the model will be 3D-printed. The control group will include patients for whom the pre-operative information will be made based on standardized information letter from the French Urological Association. Before surgery, during a preoperative therapeutic education consultation, 3D models will be presented to the patients according to the allocated study group. All patients will have to complete questionnaires to assess their anxiety level, their quality of life, their health literacy level and their understanding of disease and surgical procedure. One month after surgery, during the post-operative consultation, patients will also fill out the different questionnaires to assess their anxiety level, quality of life, and level of litteracy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tumoral Kidney
Keywords
Kidney Neoplasms, Renal-Cell Carcinoma, Nephron-Sparing Surgery, 3D Modeling, 3D Printing, Anxiety, STAI, Personalized Medicine

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
192 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Virtual 3D model group
Arm Type
Active Comparator
Arm Description
exchange time with the virtual 3D model of the kidney to be operated on as information support
Arm Title
3D Printed Model Group
Arm Type
Active Comparator
Arm Description
eexchange time with the printed three-dimensional model of the kidney to be operated on as information support
Arm Title
Control group
Arm Type
No Intervention
Arm Description
discussion time with the patient information sheet of the French Association of Urology (AFU) as information support
Intervention Type
Other
Intervention Name(s)
3D model pré-operative education
Intervention Description
Before surgery, during a preoperative therapeutic education consultation, 3D models will be presented to the patients according to the allocated study group
Primary Outcome Measure Information:
Title
Measurement of the mean pre-operative anxiety score per arm, by filling the STAI-state self-questionnaire
Description
The STAI-Etat will be collected before surgery to evaluate the effect of using a personalized three-dimensional model of the patient's kidney during a pre-operative information visit .
Time Frame
Day-1 from surgery
Secondary Outcome Measure Information:
Title
Measurement of the progression of the mean anxiety score per arm, by filling STAI-Trait Anxiety self-questionnaire.
Description
The progression of the mean anxiety score per arm, measured by STAI-State self-questionnaire at the three follow-up visits in the study and adjusted on the STAI-Trait score at baseline will assess feelings of apprehension, tension, nervousness and worries that the subject usually feels.
Time Frame
between baseline and Day 15 post-op
Title
Measurement of the progression in mean health literacy questionnaire score HLSEU-Q16 between baseline and 15-day post-operative follow-up per arm
Description
This questionnaire is a short version version of the European Health Literacy Survey Questionnaire based on a model including 4 health information processing skills: accessing, understanding, evaluating and applying application of health information .
Time Frame
between baseline and Day 15 post-op
Title
Measurement of the mean pre-operative score for understanding disease and choice of treatment per arm by filling the WAKE questionnaire
Description
The WAKE questionnaire is used assess the feeling of understanding of the disease and the choice of treatment preoperatively in each of the three groups, the questionnaire comprises five question on the understanding of the disease . Each dimension has 5 levels : very poor, poor,faire, good, very good or strongly desagree, disagree,neutral,agree or strongly agree
Time Frame
Day-1 from surgery
Title
Measurement of the progression of quality of life in each of the three groups by filling the EQ-5D-5L questionnaire
Description
The EQ-5D-5L questionnaire measures participants' quality of life.The descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. Additinonally, the questionnaire records the patient's self-rated health on a vertical visual analogue scale, where the endpoints are labelled 'The best health you can imagine' and 'The worst health you can imagine'.
Time Frame
between inclusion and Day 15 post-op
Title
Measurement of the average duration of the pre-operative information visit in each of the three groups
Time Frame
between Day-21 and Day-4 from surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients (≥ 18 years of age) Scheduled surgical management by laparoscopic partial nephrectomy with robotic assistance for kidney tumor Unilateral kidney tumor or 1st surgery for bilateral involvement Consent expressed for integration of the UroCCR cohort, Expressed consent for participation in the 3D Anxiety study. Patients affiliated or benefiting from a social security plan Exclusion Criteria: Refusal of consent or participation Difficulty understanding and expressing oneself in French Patient under guardianship or curatorship No preoperative CT scan available for 3D modeling
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jean-Christophe BERNHARD, Professeur
Phone
05 57 82 03 50
Email
jean-christophe.bernhard@chu-bordeaux.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Christophe BERNHARD, Professeur
Organizational Affiliation
University Hospital, Bordeaux
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU d'ANGERS
City
Angers
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pierre BIGOT, Pr.
Facility Name
CHU de Bordeaux
City
Bordeaux
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jean-Christophe BERNHARD, Pr.
Facility Name
CHU de CAEN
City
Caen
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Thibaut WAECKEL, Dr.
Facility Name
Hôpital Kremlin-Bicêtre
City
Le Kremlin-Bicêtre
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sébastien PARIER, Dr.
Facility Name
CHU de La CONCEPTION
City
Marseille
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Romain BOISSIER, Pr.
Facility Name
CHU de NANTES
City
Nantes
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stéphane De VERGIE, Dr.

12. IPD Sharing Statement

Learn more about this trial

Effect on Pre-operative Anxiety of a Personalized Three-dimensional Kidney Model Prior to Nephron-sparing Surgery- Rein 3D Anxiety

We'll reach out to this number within 24 hrs