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ReMindCare App for Patients From First Episode of Psychosis Unit.

Primary Purpose

Psychosis, Schizophrenia, Psychotic Disorders

Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
ReMindCare Intervention Group
Treatment as Usual
Sponsored by
INCLIVA
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Psychosis focused on measuring eHealth, mHealth, smartphone, app, psychosis, adherence, early intervention

Eligibility Criteria

17 Years - 65 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients from the FEPU at Clinic Hospital of Valencia.
  • Diagnosis of Psychotic Disorder following DSMI-5 [32] criteria.
  • Age between 17 to 65 years old.
  • Owning a smartphone which allows the correct installation and functioning of the App.
  • Owning a smartphone which allows internet connection (not necessary permanent)

Exclusion Criteria:

  • Severe Mental Disability
  • Lack of abilities in using and mastering mobile devices and internet.
  • Not to sign informed consent sheet.
  • Level of Spanish not fluid.
  • Do not have an own smartphone.

Sites / Locations

  • INCLIVA

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

ReMindCare Intervention Group

Treatment as Usual

Arm Description

Patients from First Episode of Psychosis Unit who will use ReMindCare app. ReMindCare is an user-friendly app which conducts daily evaluations of the health status of patients with psychosis by some quick questions that patients will have to answer.

Patients from First Episode of Psychosis Unit who will follow psychiatric usual care.

Outcomes

Primary Outcome Measures

Adherence to anti-psychotic treatment
Adherence to anti-psychotic medication intake. Measured by: Simplified Medication Adherence Questionnaire (SMAQ).
Adherence to treatment
Number of hospital admissions and urgent care visits
Early relapse detection
Changes in detection of relapses into psychotic sympthoms. Measured by number of contacts to patients in response to alerts generated by the app.

Secondary Outcome Measures

Alliance between patient and clinician
Changes in feelings of alliance between patient and clinician. Measured by a Satisfaction Questionnaire, made for the purpose of this research.
Feeling of empowerment related to illness self-management
Changes in patient´s feelings of empowerment related to illness self-management. Measured by a Satisfaction Questionnaire, made for the purpose of this research.
Changes in comunication between clinicians
Study of changes related to comunication between clinicians about treatment of patients. Measured qualitatively by a focus group session.

Full Information

First Posted
January 8, 2019
Last Updated
January 15, 2019
Sponsor
INCLIVA
Collaborators
Instituto de Investigacion Sanitaria INCLIVA, University of Valencia, Universitat Politècnica de València, Hospital Clínico Universitario de Valencia
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1. Study Identification

Unique Protocol Identification Number
NCT03807388
Brief Title
ReMindCare App for Patients From First Episode of Psychosis Unit.
Official Title
The Use of ReMindCare Application for Smartphone in Treatment of Patients From First Episode of Psychosis Unit in the Clinic Hospital of Valencia, Spain.
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Unknown status
Study Start Date
September 2019 (Anticipated)
Primary Completion Date
May 2020 (Anticipated)
Study Completion Date
September 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
INCLIVA
Collaborators
Instituto de Investigacion Sanitaria INCLIVA, University of Valencia, Universitat Politècnica de València, Hospital Clínico Universitario de Valencia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
ReMindCare is an app designed by the Unit of Psychiatry at the Clinical Hospital of Valencia in liaison with the Polytechnic University of Valencia. This e-Health app gathers information about the clinical health status of patients with Psychotic Disorder Diagnose through daily and weekly brief assessments. This information is displayed in a restricted access website, where clinicians can visualize data from patients as well as download pdf reports of main data collected by the app. These reports can be attached to the electronic clinical report of the patient at the hospital database, being accessible for consultation for every clinician involved in treatment of the patient. Furthermore, ReMindCare produces different alarms which notify clinicians about variations into patients health status or the cessation of using the app. Moreover, patients can also deliberately generate an urgent consultation alarm. The introduction of ReMindCare app into clinical practice will follow a clinical trial structure in which treatment as usual (TAU) of patients from a First Episode of Psychosis Unit will be compared to ReMindCare app intervention program. After participants eligible for inclusion complete baseline assessments they will be randomly allocated to one of the two groups (Intervention or TAU) by a basic single blind randomization in which an independent researcher will perform the allocation using a computerized random number generator. Information collected through the app and variations into clinical data will be analyzed among time. First assessment of these data will be conducted after 6 months of patient´s enrollment into the study. Subsequent analysis will be conducted yearly.
Detailed Description
Baseline surveys: Baseline surveys will be administered. In this first evaluation, sociodemographic information and clinical information such as diagnosis, pattern of antipsychotic treatment, number of suicide attempts or associated illnesses will be collected. Furthermore, some structured questionnaires will be administered, including: Clinical Global Impression Scale (CGI), Global Assessment of Functioning (GAF), Positive and Negative Syndrome Scale (PANSS), Premorbid Adjustment Scale (PAS), Simplified Medication Adherence Questionnaire (SMAQ), Drug Attitude Inventory (DAI-10) and Beck Cognitive Insight Scale (BCIS). ReMindCare app measures: Patients will generate the following data by using the app: Data generated through responses to daily and weekly app questionnaires: Answers to these questionnaires are presented following a Likert scale (1 to 5) as follows: 1=Not at all, 2=Slightly, 3=Somewhat, 4=Very, 5=Extremely. Responses will be collected and analyzed. Quantity of "Urgent clinic consultation" request made for every patient. Quantity of automatic usage alarms. Treatment measures: Apart from data collected through the use of the app, further information will be collected related to modifications into de patient´s treatment or related to his/her health status: Modifications into antipsychotic treatment. Number of relapses Number of visits to hospital urgent care unit. Number of hospital admissions Follow-up measures and satisfaction questionnaire: Information collected through the app and variations into clinical data will be analyzed among time. First assessment of these data will be conducted after 6 months of patient´s enrollment into the study. Subsequent analysis will be conducted yearly. Patients will also complete a satisfaction questionnaire after one year using the ReMindCare app or before discontinuing the use the app (if this happens before the first year of use of the app has come). This app feedback questionnaire is made for the purpose of this research and it is based in some previous satisfaction and usability questionnaires such as: User Version of the mobile application rating scale (uMars), System Usability Scale (SUS), EnLight: Tool for mobile and web-based eHealth interventions and App Quality Evaluation (AQEL).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Psychosis, Schizophrenia, Psychotic Disorders, Delirium, Hallucinations, Adherence, Medication, Treatment Side Effects
Keywords
eHealth, mHealth, smartphone, app, psychosis, adherence, early intervention

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
140 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
ReMindCare Intervention Group
Arm Type
Experimental
Arm Description
Patients from First Episode of Psychosis Unit who will use ReMindCare app. ReMindCare is an user-friendly app which conducts daily evaluations of the health status of patients with psychosis by some quick questions that patients will have to answer.
Arm Title
Treatment as Usual
Arm Type
Other
Arm Description
Patients from First Episode of Psychosis Unit who will follow psychiatric usual care.
Intervention Type
Device
Intervention Name(s)
ReMindCare Intervention Group
Other Intervention Name(s)
ReMindCare app
Intervention Description
Daily and weekly assessments of patient´s health status, and generation of alarms related to these answers. Moreover, patients can contact clinicians by an urgent consultation tab.
Intervention Type
Other
Intervention Name(s)
Treatment as Usual
Intervention Description
Psychiatric usual treatment at First Episode of Psychosis Unit at Clinical Hospital of Valencia, Spain.
Primary Outcome Measure Information:
Title
Adherence to anti-psychotic treatment
Description
Adherence to anti-psychotic medication intake. Measured by: Simplified Medication Adherence Questionnaire (SMAQ).
Time Frame
Yearly, up to 2 years
Title
Adherence to treatment
Description
Number of hospital admissions and urgent care visits
Time Frame
Yearly, up to 2 years
Title
Early relapse detection
Description
Changes in detection of relapses into psychotic sympthoms. Measured by number of contacts to patients in response to alerts generated by the app.
Time Frame
Yearly, up to 2 years
Secondary Outcome Measure Information:
Title
Alliance between patient and clinician
Description
Changes in feelings of alliance between patient and clinician. Measured by a Satisfaction Questionnaire, made for the purpose of this research.
Time Frame
Yearly, up to 2 years
Title
Feeling of empowerment related to illness self-management
Description
Changes in patient´s feelings of empowerment related to illness self-management. Measured by a Satisfaction Questionnaire, made for the purpose of this research.
Time Frame
Yearly, up to 2 years
Title
Changes in comunication between clinicians
Description
Study of changes related to comunication between clinicians about treatment of patients. Measured qualitatively by a focus group session.
Time Frame
Yearly, up to 2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
17 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients from the FEPU at Clinic Hospital of Valencia. Diagnosis of Psychotic Disorder following DSMI-5 [32] criteria. Age between 17 to 65 years old. Owning a smartphone which allows the correct installation and functioning of the App. Owning a smartphone which allows internet connection (not necessary permanent) Exclusion Criteria: Severe Mental Disability Lack of abilities in using and mastering mobile devices and internet. Not to sign informed consent sheet. Level of Spanish not fluid. Do not have an own smartphone.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lucia Bonet, PhD
Phone
+34 600745550
Email
lbonetm@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Julio Sanjuán
Organizational Affiliation
INCLIVA
Official's Role
Study Director
Facility Information:
Facility Name
INCLIVA
City
Valencia
ZIP/Postal Code
46010
Country
Spain
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marta Peiró

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
We plan to share the following IPD data. However they will be analyzed as a group: Responses to the following questionnaires: Clinical Global Impression Scale (CGI) Global Assessment of Functioning (GAF) Positive and Negative Syndrome Scale (PANSS) Simplified Medication Adherence Questionnaire (SMAQ) Drug Attitude Inventory (DAI-10) Beck Cognitive Insight Scale (BCIS) Socio-demographics information such as: Age, gender, ethnicity education, marital status, living situation. Answers of patient to ReMindCare app assessments: Daily / weekly responses and alarms generated Treatment related measures: Modifications into antipsychotic treatment. Number of relapses Number of visits to hospital urgent care unit. Number of hospital admissions
IPD Sharing Time Frame
The data has been sent for publication in an open access journal.
Citations:
PubMed Identifier
28258835
Citation
Bonet L, Izquierdo C, Escarti MJ, Sancho JV, Arce D, Blanquer I, Sanjuan J. Use of mobile technologies in patients with psychosis: A systematic review. Rev Psiquiatr Salud Ment. 2017 Jul-Sep;10(3):168-178. doi: 10.1016/j.rpsm.2017.01.003. Epub 2017 Mar 1. English, Spanish.
Results Reference
background
PubMed Identifier
30045835
Citation
Bonet L, Llacer B, Hernandez-Viadel M, Arce D, Blanquer I, Canete C, Escarti M, Gonzalez-Pinto AM, Sanjuan J. Differences in the Use and Opinions About New eHealth Technologies Among Patients With Psychosis: Structured Questionnaire. JMIR Ment Health. 2018 Jul 25;5(3):e51. doi: 10.2196/mental.9950.
Results Reference
background

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ReMindCare App for Patients From First Episode of Psychosis Unit.

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