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Multicomponent Strategy to Implement a Clinical Practice Guideline and Improve Health Outcomes in People With SLE

Primary Purpose

Systemic Lupus Erythematosus

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Multicomponent intervention
Sponsored by
Servicio Canario de Salud
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Systemic Lupus Erythematosus focused on measuring Lupus, Quality of life, Multicomponent intervention, Clinical Practice Guideline, Computerized clinical decision support system, Activity

Eligibility Criteria

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

Inclusion Criteria:

  • Patients:

Adults (older than 18 years) diagnosed with SLE of any seriousness and situation (active, remission or clinically quiescent and serologically active), who agree to participate and sign informed consent.

  • Health professionals:

Physicians specialized in rheumatology or internal medicine that include in their quotas a minimum of 30 patients with eligible SLE.

Exclusion Criteria:

  • Patients:

SLE limited to the skin, advanced chronic kidney disease (dialysis or renal transplant); Mental illnesses and / or sensory or cognitive deficits; or participating in extension or follow-up studies of another RCT (possible change in follow-up guidelines). Participants in observational studies may be included as they do not change usual practice.

Sites / Locations

  • Servicio de Evaluación del Servicio Canario de la Salud

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Multicomponent Intervention

Control

Arm Description

Rheumatologist and internist receive a multicomponent intervention

Rheumatologist and internist provide the usual care

Outcomes

Primary Outcome Measures

Change of self-perceived activity of the SLE
Disease activity self-reported by the patient using the Systemic Lupus Erythematosus Activity (SLAQ) Questionnaire

Secondary Outcome Measures

Change in professional's knowledge about SLE management
Acquired knowledges assessed by a questionnaire designed ad hoc
Change in self-perceived health-related quality of life
Self-perceived health-related quality of life using EQ-5D - 5L questionnaire
Change in self-perceived health-related quality of life
Self-perceived health-related quality of life using LupusQol questionnaire
Patient's perception of their participation in decision making
Patient's perception of clinician facilitation and decision-making process using the Shared Decision-Making (SDM-Q-9) Questionnaire
Professional's attitude to partnership with the patient for shared decision making
Professionals' attitudes towards shared decision making assessed by the Leeds Attitude Towards Concordance II Scale (LATCon II)
Professionals' adherence to CPG-SLE recommendations
Degree of professional adherence to recommendations will be determined through data collection from clinical records in terms of percentage of patients with adequate treatment according to SLE-CPG recommendations

Full Information

First Posted
April 16, 2018
Last Updated
September 21, 2021
Sponsor
Servicio Canario de Salud
Collaborators
Instituto de Salud Carlos III
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1. Study Identification

Unique Protocol Identification Number
NCT03537638
Brief Title
Multicomponent Strategy to Implement a Clinical Practice Guideline and Improve Health Outcomes in People With SLE
Official Title
Effectiveness and Cost-effectiveness of a Multicomponent Strategy to Implement a Clinical Practice Guideline and Improve Health Outcomes in People With Systemic Lupus Erythematosus
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
April 16, 2018 (Actual)
Primary Completion Date
October 19, 2020 (Actual)
Study Completion Date
December 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Servicio Canario de Salud
Collaborators
Instituto de Salud Carlos III

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
Principal objective: To produce scientific knowledge on the effectiveness and cost-effectiveness of a multicomponent intervention for knowledge transfer and implementing a Clinical Practice Guideline (CPG) for Systemic Lupus Erythematosus (SLE), formed by an educative intervention, an computerized clinical decision support system (SADC), complemented by an automated feedback built into the electronic clinical record. Secondary objectives will be previously developed: 1) the analysis of medical practice variations along the care of SLE patients in the Canary Islands Health Service (SCS); 2) the best available scientific evidence to support the optimal development of the SADC; 3) the context and the barriers to innovation implementation in the SCS; and 4) the development of the contents for the implementation strategy, including the SADC and the automated feedback. Methods for the main objective: The main objective will be assessed under an open, multicentric and randomized (by clusters) clinical trial, in the SCS. The multicomponent intervention will be compared to the usual procedures for CPG dissemination. The main measure will be the self-perceived activity of SLE rated by the SLAQ scale. Self-perceived health related quality of life (HRQoL) data will be obtained by means of the questionnaire EQ-5D-5L , to estimate a cost-effectiveness ratio. Methods for secondary objectives: The rest of the objectives will be developed by a mix of quantitative and qualitative research methods to allow adapting the design, development and execution of the intervention to the characteristics of the context.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Systemic Lupus Erythematosus
Keywords
Lupus, Quality of life, Multicomponent intervention, Clinical Practice Guideline, Computerized clinical decision support system, Activity

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
237 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Multicomponent Intervention
Arm Type
Experimental
Arm Description
Rheumatologist and internist receive a multicomponent intervention
Arm Title
Control
Arm Type
No Intervention
Arm Description
Rheumatologist and internist provide the usual care
Intervention Type
Behavioral
Intervention Name(s)
Multicomponent intervention
Intervention Description
Intervention to rheumatologist and internist responsible for the care of patients with SLE. Implementation multicomponent intervention consisting of: educational component, a computerized clinical decision support system developed from the clinical practice guide - SLE and automated feedback integrated into the electronic medical record system.
Primary Outcome Measure Information:
Title
Change of self-perceived activity of the SLE
Description
Disease activity self-reported by the patient using the Systemic Lupus Erythematosus Activity (SLAQ) Questionnaire
Time Frame
18 months
Secondary Outcome Measure Information:
Title
Change in professional's knowledge about SLE management
Description
Acquired knowledges assessed by a questionnaire designed ad hoc
Time Frame
18 months
Title
Change in self-perceived health-related quality of life
Description
Self-perceived health-related quality of life using EQ-5D - 5L questionnaire
Time Frame
18 months
Title
Change in self-perceived health-related quality of life
Description
Self-perceived health-related quality of life using LupusQol questionnaire
Time Frame
18 months
Title
Patient's perception of their participation in decision making
Description
Patient's perception of clinician facilitation and decision-making process using the Shared Decision-Making (SDM-Q-9) Questionnaire
Time Frame
18 months
Title
Professional's attitude to partnership with the patient for shared decision making
Description
Professionals' attitudes towards shared decision making assessed by the Leeds Attitude Towards Concordance II Scale (LATCon II)
Time Frame
18 months
Title
Professionals' adherence to CPG-SLE recommendations
Description
Degree of professional adherence to recommendations will be determined through data collection from clinical records in terms of percentage of patients with adequate treatment according to SLE-CPG recommendations
Time Frame
18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients: Adults (older than 18 years) diagnosed with SLE of any seriousness and situation (active, remission or clinically quiescent and serologically active), who agree to participate and sign informed consent. Health professionals: Physicians specialized in rheumatology or internal medicine that include in their quotas a minimum of 30 patients with eligible SLE. Exclusion Criteria: Patients: SLE limited to the skin, advanced chronic kidney disease (dialysis or renal transplant); Mental illnesses and / or sensory or cognitive deficits; or participating in extension or follow-up studies of another RCT (possible change in follow-up guidelines). Participants in observational studies may be included as they do not change usual practice.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
María de Mar Trujillo Martin, PhD
Organizational Affiliation
Servicio de Evaluación del Servicio Canario de la Salud
Official's Role
Principal Investigator
Facility Information:
Facility Name
Servicio de Evaluación del Servicio Canario de la Salud
City
Santa Cruz de Tenerife
ZIP/Postal Code
38004
Country
Spain

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Multicomponent Strategy to Implement a Clinical Practice Guideline and Improve Health Outcomes in People With SLE

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