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Feasibility and Preliminary Effectiveness of a Shared Decision-making Process

Primary Purpose

Clinical Decision Making, Patient-Centered Care, Obesity

Status
Recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Shared decision-making model
Sponsored by
Hospital Vall d'Hebron
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Clinical Decision Making

Eligibility Criteria

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

Inclusion Criteria Obesity:

  • Adult patients, between 18 and 60 years old, Spanish or Catalan speakers, who have scheduled a visit to the obesity clinic.
  • BMI≥40Kg/m2 or ≥35kg/m2 with major associated comorbidities, likely to improve after weight loss
  • Presence of morbid obesity established for at least five years
  • Absence of endocrine disorders that cause obesity
  • Favorable psychiatric-psychological evaluation
  • Informed consent to participate in the study after having received all the necessary information (oral and written)

Exclusion Criteria Obesity:

  • Patient with cognitive impairment that does not allow for a shared decision-making process.
  • Unstable organic disease limiting the probability of success and benefit of participation in the obesity unit program.
  • Patients previously operated on bariatric surgery
  • Clinical contraindications included in the general criteria of the Bariatric Surgery Protocol of the Hospital Universitari Vall d'Hebron
  • Clinical contraindications for pharmacological treatment according to technical date of GLP-1 analogues (Trulicity, Ozempic, Victoza, Saxenda)

Inclusion Criteria ACKD:

  • Adult patients aged 18 or over who speak Spanish or Catalan who have a scheduled visit to the ACKD clinic.
  • Advanced chronic kidney disease (GFR ≤20ml/min) that requires assessment of the start of renal replacement therapy through any dialysis, transplant or conservative treatment.
  • Informed consent to participate in the study after having received all the necessary information (oral and written)

Exclusion Criteria ACKD:

  • Having previously performed any modality of renal replacement therapy.
  • Patient with cognitive impairment that does not allow for a shared decision-making process.

Sites / Locations

  • Hospital Vall d'HebronRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Shared decision-making model

Usual care

Arm Description

In the intervention group, the shared decision-making model will be carried out. This model was proposed and designed through a participatory and deliberative process.

Information without an estructured shared decision-making model

Outcomes

Primary Outcome Measures

Feasibility of the decision-making model
The number of patients in the intervention group agreed to participate in a shared decision-making process and complete the entire process until answering the questionnaires. A value of ≥80% of the intervention group will be considered viable
Preliminary effectiveness - Knowledge
Measured through multiple-choice questions proposed by the study researchers. We will measure the number of correct answers in both groups
Preliminary effectiveness - Satisfaction with decision
Measured with the self-reported Satisfaction With Decision scale (SWDs) (6 items with 5-item Likert scales)
Preliminary effectiveness - Perception of shared decision-making process
Measures patients' perceptions of how clinicians' performance fits the shared decision-making process. We will use the self-reported 9-item Shared Decision-Making Questionnaire (9 items with 6-item Likert scale)
Preliminary effectiveness - Decisional conflict
Measured with the self-reported Decisional Conflict Scale (16 items with 5-item Likert scale)
Preliminary effectiveness - Perception of participation in the decision-making process
Measured with the CollaboRATE scale (3 item self-report questions, range from 0 to 7

Secondary Outcome Measures

Decision made
Number of participants that choose one option: Obesity group: surgical intervention vs medical treatment ACKD group: hemodialysis vs peritoneal dialysis vs conservative care
Duration of each medical visit
We will measure, in minutes, the total time of clinical encounters for both groups
Number of visits necessary until the final decision is made
number of visits

Full Information

First Posted
June 15, 2022
Last Updated
August 1, 2022
Sponsor
Hospital Vall d'Hebron
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1. Study Identification

Unique Protocol Identification Number
NCT05424809
Brief Title
Feasibility and Preliminary Effectiveness of a Shared Decision-making Process
Official Title
Feasibility and Preliminary Effectiveness of a Shared Decision-making Process in a Tertiary University Hospital: Protocol of a Pilot Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Recruiting
Study Start Date
May 20, 2022 (Actual)
Primary Completion Date
November 23, 2022 (Anticipated)
Study Completion Date
December 23, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Vall d'Hebron

4. Oversight

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

5. Study Description

Brief Summary
Background: Shared decision-making is a process where health professionals and patients work together through conversation and using tools to make the best possible decision for the person. Patient decision aids provide information based on the best available evidence, support the deliberative process, and further help clarifies individual patient values and preferences. Incorporating shared decision-making in clinical practice is challenging. Hypothesis: A proposed shared decision-making implementation model is feasible and improves patients' knowledge of possible treatment options, as well as patients' perception and degree of satisfaction with the decision-making process. Objective: To evaluate the feasibility and preliminary effectiveness of implementing a shared decision-making model in a tertiary university hospital. Methods: It is proposed to carry out a pilot randomized clinical study (ratio 1:1), with two arms, in parallel, open, single center. Adult patients from two clinical processes will be included: a) Obesity (treatment options: bariatric surgery or medical management (healthy habits +/- pharmacological treatment), and b) Advanced Chronic Kidney Disease (ACKD) (treatment options: hemodialysis, peritoneal dialysis, or conservative treatment). Since it is a pilot study, the investigators estimated a random sample of between 20 to 40 participants per intervention group and control group (total sample 40 to 80 per pathology) would be needed. The intervention group will carry out the shared decision-making model, and the control group will receive the usual clinical practice with detailed information from a health professional. The primary outcomes of interest to be evaluated are a) feasibility; b) quality of the decision and the decision-making process.
Detailed Description
Background: Shared decision-making is a process where health professionals and patients work together through conversation and using tools to make the best possible decision for the person. Patient decision aids provide information based on the best available evidence, support the deliberative process, and further help clarifies individual patient values and preferences. Incorporating shared decision-making in clinical practice is challenging. Some studies have analyzed the implementation of shared decision-making in specific clinical processes. However, the investigators have only been able to identify one study, still in progress, that plans to implement and evaluate the integration of a shared decision-making program in a university hospital. Hypothesis: The proposed shared decision-making implementation model is feasible and improves patients' knowledge of possible treatment options, as well as patients' perception and degree of satisfaction with the decision-making process. Objective: To evaluate the feasibility and preliminary effectiveness of implementing a shared decision-making model in a tertiary university hospital. Methods: It is proposed to carry out a pilot randomized clinical study (ratio 1:1), with two arms, in parallel, open, single center. The guidelines of the 2010 CONSORT statement for reporting randomized trials will be followed. Adult patients from two clinical processes will be included: a) Obesity (treatment options: bariatric surgery or medical management (healthy habits +/- pharmacological treatment), and b) Advanced Chronic Kidney Disease (ACKD) (treatment options to decide: hemodialysis, peritoneal dialysis, or conservative treatment). Since it is a pilot study, the investigators estimated a random sample of between 20 to 40 participants per intervention group and control group (total sample 40 to 80 per pathology) would be needed. The intervention group will carry out the shared decision-making model, and the control group will receive the usual clinical practice with detailed information from a health professional. The outcomes of interest to be evaluated are a) feasibility (defined by the number of patients in the intervention group who agree to participate in a shared decision-making process and who complete the entire study process); b) quality of the decision and the decision-making process (defined by the degree of knowledge, scale of satisfaction with the decision, quality of the process, decisional conflict and perception of information and inclusion in the process). The recruitment of patients will begin in May 2022. The assignment of patients in Obesity will be carried out from the Agenda Service, where a person outside the research team will randomly assign each patient to the first visit of the intervention group or control group. In ACKD, the assignment will be randomly through the REDCap computer program. The coded collection of variables will also be carried out through the REDCap program.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Clinical Decision Making, Patient-Centered Care, Obesity, Chronic Kidney Diseases

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Shared decision-making model
Arm Type
Experimental
Arm Description
In the intervention group, the shared decision-making model will be carried out. This model was proposed and designed through a participatory and deliberative process.
Arm Title
Usual care
Arm Type
No Intervention
Arm Description
Information without an estructured shared decision-making model
Intervention Type
Behavioral
Intervention Name(s)
Shared decision-making model
Intervention Description
The model is based on a person-centred care process, where an exchange of information is carried out between the health professional and the patient to make the best decision that is consistent with the person's values and preferences. A six-stage process constitutes the model: 1) Identificacion of the decision point, 2) design of a specific patient decision aid, 3) identification of possible barriers and ways to overcome them, 4) training for professionals, 5) 3-steps implementation of shared decision-making in clinical practice, 6) evaluation
Primary Outcome Measure Information:
Title
Feasibility of the decision-making model
Description
The number of patients in the intervention group agreed to participate in a shared decision-making process and complete the entire process until answering the questionnaires. A value of ≥80% of the intervention group will be considered viable
Time Frame
4-6 weeks
Title
Preliminary effectiveness - Knowledge
Description
Measured through multiple-choice questions proposed by the study researchers. We will measure the number of correct answers in both groups
Time Frame
4-6 weeks
Title
Preliminary effectiveness - Satisfaction with decision
Description
Measured with the self-reported Satisfaction With Decision scale (SWDs) (6 items with 5-item Likert scales)
Time Frame
4-6 weeks
Title
Preliminary effectiveness - Perception of shared decision-making process
Description
Measures patients' perceptions of how clinicians' performance fits the shared decision-making process. We will use the self-reported 9-item Shared Decision-Making Questionnaire (9 items with 6-item Likert scale)
Time Frame
4-6 weeks
Title
Preliminary effectiveness - Decisional conflict
Description
Measured with the self-reported Decisional Conflict Scale (16 items with 5-item Likert scale)
Time Frame
4-6 weeks
Title
Preliminary effectiveness - Perception of participation in the decision-making process
Description
Measured with the CollaboRATE scale (3 item self-report questions, range from 0 to 7
Time Frame
4-6 weeks
Secondary Outcome Measure Information:
Title
Decision made
Description
Number of participants that choose one option: Obesity group: surgical intervention vs medical treatment ACKD group: hemodialysis vs peritoneal dialysis vs conservative care
Time Frame
4-6 weeks
Title
Duration of each medical visit
Description
We will measure, in minutes, the total time of clinical encounters for both groups
Time Frame
4-6 weeks
Title
Number of visits necessary until the final decision is made
Description
number of visits
Time Frame
4-6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Obesity: Adult patients, between 18 and 60 years old, Spanish or Catalan speakers, who have scheduled a visit to the obesity clinic. BMI≥40Kg/m2 or ≥35kg/m2 with major associated comorbidities, likely to improve after weight loss Presence of morbid obesity established for at least five years Absence of endocrine disorders that cause obesity Favorable psychiatric-psychological evaluation Informed consent to participate in the study after having received all the necessary information (oral and written) Exclusion Criteria Obesity: Patient with cognitive impairment that does not allow for a shared decision-making process. Unstable organic disease limiting the probability of success and benefit of participation in the obesity unit program. Patients previously operated on bariatric surgery Clinical contraindications included in the general criteria of the Bariatric Surgery Protocol of the Hospital Universitari Vall d'Hebron Clinical contraindications for pharmacological treatment according to technical date of GLP-1 analogues (Trulicity, Ozempic, Victoza, Saxenda) Inclusion Criteria ACKD: Adult patients aged 18 or over who speak Spanish or Catalan who have a scheduled visit to the ACKD clinic. Advanced chronic kidney disease (GFR ≤20ml/min) that requires assessment of the start of renal replacement therapy through any dialysis, transplant or conservative treatment. Informed consent to participate in the study after having received all the necessary information (oral and written) Exclusion Criteria ACKD: Having previously performed any modality of renal replacement therapy. Patient with cognitive impairment that does not allow for a shared decision-making process.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Karla Salas-Gama, MD
Phone
+34667117798
Email
karla.salas@vallhebron.cat
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Karla Salas Gama, MD
Organizational Affiliation
Hospital Vall d'Hebron
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Vall d'Hebron
City
Barcelona
ZIP/Postal Code
08023
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Karla Salas-Gama, MD
Phone
+34667117798
Email
karla.salas@vallhebron.cat

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
27121606
Citation
Fearns N, Kelly J, Callaghan M, Graham K, Loudon K, Harbour R, Santesso N, McFarlane E, Thornton J, Treweek S. What do patients and the public know about clinical practice guidelines and what do they want from them? A qualitative study. BMC Health Serv Res. 2016 Feb 24;16:74. doi: 10.1186/s12913-016-1319-4.
Results Reference
background
PubMed Identifier
28402085
Citation
Stacey D, Legare F, Lewis K, Barry MJ, Bennett CL, Eden KB, Holmes-Rovner M, Llewellyn-Thomas H, Lyddiatt A, Thomson R, Trevena L. Decision aids for people facing health treatment or screening decisions. Cochrane Database Syst Rev. 2017 Apr 12;4(4):CD001431. doi: 10.1002/14651858.CD001431.pub5.
Results Reference
background
PubMed Identifier
22618581
Citation
Elwyn G, Frosch D, Thomson R, Joseph-Williams N, Lloyd A, Kinnersley P, Cording E, Tomson D, Dodd C, Rollnick S, Edwards A, Barry M. Shared decision making: a model for clinical practice. J Gen Intern Med. 2012 Oct;27(10):1361-7. doi: 10.1007/s11606-012-2077-6. Epub 2012 May 23.
Results Reference
background
PubMed Identifier
30025154
Citation
Legare F, Adekpedjou R, Stacey D, Turcotte S, Kryworuchko J, Graham ID, Lyddiatt A, Politi MC, Thomson R, Elwyn G, Donner-Banzhoff N. Interventions for increasing the use of shared decision making by healthcare professionals. Cochrane Database Syst Rev. 2018 Jul 19;7(7):CD006732. doi: 10.1002/14651858.CD006732.pub4.
Results Reference
background
PubMed Identifier
31129012
Citation
Sondergaard SR, Madsen PH, Hilberg O, Jensen KM, Olling K, Steffensen KD. A prospective cohort study of shared decision making in lung cancer diagnostics: Impact of using a patient decision aid. Patient Educ Couns. 2019 Nov;102(11):1961-1968. doi: 10.1016/j.pec.2019.05.018. Epub 2019 May 16.
Results Reference
background
PubMed Identifier
29641952
Citation
Steffensen KD, Vinter M, Cruger D, Dankl K, Coulter A, Stuart B, Berry LL. Lessons in Integrating Shared Decision-Making Into Cancer Care. J Oncol Pract. 2018 Apr;14(4):229-235. doi: 10.1200/JOP.18.00019.
Results Reference
background
PubMed Identifier
33039998
Citation
Danner M, Geiger F, Wehkamp K, Rueffer JU, Kuch C, Sundmacher L, Skjelbakken T, Rummer A, Novelli A, Debrouwere M, Scheibler F; SHARE TO CARE (S2C) Project Team. Making shared decision-making (SDM) a reality: protocol of a large-scale long-term SDM implementation programme at a Northern German University Hospital. BMJ Open. 2020 Oct 10;10(10):e037575. doi: 10.1136/bmjopen-2020-037575.
Results Reference
background
PubMed Identifier
25921323
Citation
Chabrera C, Areal J, Font A, Caro M, Bonet M, Zabalegui A. [Spanish version of the Satisfaction With Decision scale: cross-cultural adaptation, validity and reliability]. Enferm Clin. 2015 May-Jun;25(3):117-23. doi: 10.1016/j.enfcli.2015.02.005. Epub 2015 Apr 25. Spanish.
Results Reference
background
PubMed Identifier
24593044
Citation
De las Cuevas C, Perestelo-Perez L, Rivero-Santana A, Cebolla-Marti A, Scholl I, Harter M. Validation of the Spanish version of the 9-item Shared Decision-Making Questionnaire. Health Expect. 2015 Dec;18(6):2143-53. doi: 10.1111/hex.12183. Epub 2014 Mar 5.
Results Reference
background
PubMed Identifier
19301775
Citation
Urrutia M, Campos S, O'Connor A. [Validation of a Spanish version of the Decisional Conflict scale]. Rev Med Chil. 2008 Nov;136(11):1439-47. doi: 10.4067/s0034-98872008001100010. Spanish.
Results Reference
background
PubMed Identifier
28760344
Citation
Bravo P, Contreras A, Dois A, Villarroel L. [Adapting and validating the generic instrument CollaboRATE to measure women's participation in health related decision-making during the reproductive process]. Aten Primaria. 2018 May;50(5):274-281. doi: 10.1016/j.aprim.2017.04.003. Epub 2017 Jul 29. Spanish.
Results Reference
background

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Feasibility and Preliminary Effectiveness of a Shared Decision-making Process

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