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A Multi-component Intervention to Improve Medication Adherence in People With Depressive Disorders (MAPDep)

Primary Purpose

Depressive Disorder

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Intervention to Patients
Intervention to Psychiatrists
Control
Sponsored by
Servicio Canario de Salud
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Depressive Disorder focused on measuring Depression, Medication adherence, Multicomponent intervention

Eligibility Criteria

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

Inclusion Criteria:

  • Patients:

    • Patients with diagnosis of depressive disorder (major depressive disorder MDD and/or dysthymia) under pharmacological treatment
    • Regular users of mobile phones
    • Patients who have consulted their psychiatrist about their depression at least once in the previous 6 months
  • Health professionals:

Psychiatrists have no intention of moving from their practice during the study period.

Exclusion criteria:

• Patient:

  • Patients with history of current bipolar disorder and/or any psychotic disorder
  • Insufficient language skills
  • Pregnancy

Sites / Locations

  • Servicio de Evaluación. Servicio Canario de Salud

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Other

Arm Label

Intervention to Patients

Intervention to Psychiatrists

Mixed Intervention

Control

Arm Description

Only patients receive intervention

Psychiatrists receive the intervention. Their associated patients do not receive direct intervention although indirect intervention through professionals

Patients and Psychiatrists associated with these patients receive intervention

Psychiatrists provide the usual care Patients receive usual care

Outcomes

Primary Outcome Measures

Change in the Sidorkiewicz instrument score
Change in adherence from baseline to 6 months. This instrument contains 5 questions to help patients recognize their different medication-taking behaviors for each drug taken. The results generate adherence levels ranging from 1 (high drug adherence) to 6 (drug discontinuation).

Secondary Outcome Measures

Change in the Sidorkiewicz instrument score
Change in adherence from baseline to 3 and 12 months.
Change in Beck Depression Inventory - II (BDI-II) score
BDI-II contains 21 questions, each answer being scored on a scale value of 0 to 3. Higher total scores indicate more severe depressive symptoms.
Change in Hospital Anxiety and Depression Scale (HADS) score
HADS contains two 7-item Likert scales, one for anxiety and one for depression, with responses being scored on a scale of 0-3 (3 indicates higher symptom frequencies).
Change in Physical Functioning Subscale (PF-10) of the 36-item Short Form Health Survey (SF-36)
PF-10 contains 10-item Likert scale designed to examine a person's perceived limitation with physical functioning. Each item is rated on a 3-point scale (yes, limited a lot; yes, limited a little; and no, not limited at all).
Change in EQ-5D-5L
EQ-5D-5L is a questionnaire consisting of five domains (Mobility, Self-Care, Usual Activity, Pain/Discomfort and Anxiety/Depression) each with five levels (no problems, slight problems, moderate problems, severe problems and extreme problems).
Change in Patient-Practitioner Orientation Scale (PPOS) score
PPOS is a self-administered questionnaire that assesses patient-centeredness healthcare professionals. PPOS contains 18 items scored on a 6-point Likert scale (strongly disagree to strongly agree).

Full Information

First Posted
July 9, 2018
Last Updated
April 11, 2023
Sponsor
Servicio Canario de Salud
Collaborators
University of La Laguna
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1. Study Identification

Unique Protocol Identification Number
NCT03668457
Brief Title
A Multi-component Intervention to Improve Medication Adherence in People With Depressive Disorders
Acronym
MAPDep
Official Title
Effectiveness and Cost-effectiveness of a Multi-component Intervention to Improve Medication Adherence in People With Depressive Disorders
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Completed
Study Start Date
March 1, 2020 (Actual)
Primary Completion Date
November 1, 2022 (Actual)
Study Completion Date
November 1, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Servicio Canario de Salud
Collaborators
University of La Laguna

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
Objective: The study of medication adherence in depression (MAPDep study) aims to evaluate the effectiveness and cost-effectiveness of a multi-component strategy to enhance patient-centered care to improve adherence toward medications in patients with depression, formed by an educational intervention to psychiatrists and/or a collaborative care intervention group to patients and relatives plus a reminder system through the use of a mobile APP. Methods: The objective will be assessed under an open multicenter, clinical controlled trial with random allocation by clusters to one of three interventions or to usual care (control arm). In group 1 only patients and family members receive intervention, in group 2 only psychiatrists receive intervention, and group 3 is a combined intervention for patients and psychiatrists. The main measure will be the change in medication adherence rate. Secondary endpoints are depression, emotional distress, health-related quality of life, physical functioning, patients' knowledge about their medications, provider beliefs regarding patient-centeredness, and healthcare resource utilization.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depressive Disorder
Keywords
Depression, Medication adherence, Multicomponent intervention

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
170 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention to Patients
Arm Type
Experimental
Arm Description
Only patients receive intervention
Arm Title
Intervention to Psychiatrists
Arm Type
Experimental
Arm Description
Psychiatrists receive the intervention. Their associated patients do not receive direct intervention although indirect intervention through professionals
Arm Title
Mixed Intervention
Arm Type
Experimental
Arm Description
Patients and Psychiatrists associated with these patients receive intervention
Arm Title
Control
Arm Type
Other
Arm Description
Psychiatrists provide the usual care Patients receive usual care
Intervention Type
Behavioral
Intervention Name(s)
Intervention to Patients
Intervention Description
Multifaceted intervention consisting of: A collaborative care management intervention, including depression education, medication management and behavioral activation. Use of a medication reminder mobile app.
Intervention Type
Behavioral
Intervention Name(s)
Intervention to Psychiatrists
Intervention Description
Educational intervention consisting of theoretical and practical sessions to to improve communication and negotiation abilities, and to develop skills to promote patient-centered care and shared decision-making.
Intervention Type
Other
Intervention Name(s)
Control
Intervention Description
Other: Usual care Usual care for depressive disorder received in mental health units
Primary Outcome Measure Information:
Title
Change in the Sidorkiewicz instrument score
Description
Change in adherence from baseline to 6 months. This instrument contains 5 questions to help patients recognize their different medication-taking behaviors for each drug taken. The results generate adherence levels ranging from 1 (high drug adherence) to 6 (drug discontinuation).
Time Frame
Baseline and 6 months
Secondary Outcome Measure Information:
Title
Change in the Sidorkiewicz instrument score
Description
Change in adherence from baseline to 3 and 12 months.
Time Frame
Baseline, 3 and 12 months
Title
Change in Beck Depression Inventory - II (BDI-II) score
Description
BDI-II contains 21 questions, each answer being scored on a scale value of 0 to 3. Higher total scores indicate more severe depressive symptoms.
Time Frame
Baseline, 3, 6, and 12 months
Title
Change in Hospital Anxiety and Depression Scale (HADS) score
Description
HADS contains two 7-item Likert scales, one for anxiety and one for depression, with responses being scored on a scale of 0-3 (3 indicates higher symptom frequencies).
Time Frame
Baseline, 3, 6, and 12 months
Title
Change in Physical Functioning Subscale (PF-10) of the 36-item Short Form Health Survey (SF-36)
Description
PF-10 contains 10-item Likert scale designed to examine a person's perceived limitation with physical functioning. Each item is rated on a 3-point scale (yes, limited a lot; yes, limited a little; and no, not limited at all).
Time Frame
Baseline, 6, and 12 months
Title
Change in EQ-5D-5L
Description
EQ-5D-5L is a questionnaire consisting of five domains (Mobility, Self-Care, Usual Activity, Pain/Discomfort and Anxiety/Depression) each with five levels (no problems, slight problems, moderate problems, severe problems and extreme problems).
Time Frame
Baseline, 6, and 12 months
Title
Change in Patient-Practitioner Orientation Scale (PPOS) score
Description
PPOS is a self-administered questionnaire that assesses patient-centeredness healthcare professionals. PPOS contains 18 items scored on a 6-point Likert scale (strongly disagree to strongly agree).
Time Frame
Baseline and 12 months
Other Pre-specified Outcome Measures:
Title
Healthcare utilization, cost and productivity losses
Description
Costs because of the clinical management in all groups will be assessed from the healthcare services perspective, including the costs related to the development and use of all components for each intervention assessed (group sessions, app, etc.). Information about prescribed medication and doses; patient contacts with psychiatric and primary care services; hospital admissions and length of stay; and productivity losses will be obtained from a self-administered questionnaire.
Time Frame
Baseline, 6, and 12 months
Title
The Control Preferences Scale (CPS)
Description
CPS consists of five "cards" on a board, each illustrating a different role in decision-making by means of a cartoon and short descriptive statement. Patients has to choose between the cards, observing them one at a time, to establish an order of preference that ranged from a completely active role to a more passive style (from 0 to 5, where the higher the score, the more passive the style).
Time Frame
Baseline
Title
Drug Attitude Inventory (DAI)
Description
DAI is 10-item self-report scale that assesses psychiatric patients' attitudes toward their psychopharmacological medications. Response options are true/false, with scores ranging from a minimum of -10 to a maximum of 10. A positive total score means a positive attitude, while a negative total score indicates a negative attitude.
Time Frame
Baseline
Title
Form C of the Multidimensional Health Locus of Control Scales (MHLC-C)
Description
MHLC-C is an 18-item self-report scale composed of four subscales that measure control variables with regard to participants' health, with a 6-point rating scale ranging from 1 (strongly disagree) to 6 (strongly agree). Higher scores on each subscale indicate a stronger belief in that kind of control.
Time Frame
Baseline
Title
The Hong Psychological Reactance Scale (HPRS)
Description
HPRS is a 14-item self-report questionnaire designed to measure the individual difference in reactance proneness. Each item is rated on a five-point Likert scale (ranging from 1 = strongly disagree to 5 = strongly agree).
Time Frame
Baseline
Title
Beliefs about Medicines Questionnaire (BMQ)
Description
BMQ assesses patients' beliefs and worries about taking medication for their disease. It comprises a general and a specific scale.The BMQ-General scale assesses more general beliefs or social representations of pharmaceuticals as a class of treatment and includes eight items in two subscales (four items each), Overuse and Harm. The BMQ-Specific scale assesses patient's beliefs about the medication he/she is prescribed for a specific illness in terms of the necessity and concern about taking it. This scale includes ten items in two subscales (five items each), Concern and Necessity. The degree of agreement with each statement is indicated on a five-point Likert scale (ranging from 1=strongly disagree to 5=strongly agree).
Time Frame
Baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients: Patients with diagnosis of depressive disorder (major depressive disorder MDD and/or dysthymia) under pharmacological treatment Regular users of mobile phones Patients who have consulted their psychiatrist about their depression at least once in the previous 6 months Health professionals: Psychiatrists have no intention of moving from their practice during the study period. Exclusion criteria: • Patient: Patients with history of current bipolar disorder and/or any psychotic disorder Insufficient language skills Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
María del Mar Trujillo Martín, PhD
Organizational Affiliation
Servicio de Evaluación del Servicio Canario de la Salud
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Carlos de las Cuevas Castresana, MD, PhD
Organizational Affiliation
University of La Laguna
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Tasmania del Pino-Sedeño, PhD
Organizational Affiliation
University of La Laguna
Official's Role
Principal Investigator
Facility Information:
Facility Name
Servicio de Evaluación. Servicio Canario de Salud
City
Santa Cruz de Tenerife
ZIP/Postal Code
38004
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
30863020
Citation
Del Pino-Sedeno T, Penate W, de Las Cuevas C, Valcarcel-Nazco C, Fumero A, Serrano-Perez PG, Acosta Artiles FJ, Ramos Garcia V, Leon Salas B, Bejarano-Quisoboni D, Trujillo-Martin MM. Effectiveness and cost-effectiveness of a multicomponent intervention to improve medication adherence in people with depressive disorders - MAPDep: a study protocol for a cluster randomized controlled trial. Patient Prefer Adherence. 2019 Feb 22;13:309-319. doi: 10.2147/PPA.S172963. eCollection 2019.
Results Reference
derived

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A Multi-component Intervention to Improve Medication Adherence in People With Depressive Disorders

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