- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06230237
Telephone Support vs. Self-guidance in an Internet-based Self-administered Psychological Program to Address Depression
Telephone Support vs. Self-guidance in an Internet-based Self-administered Psychological Program for the Treatment of Depression
Depression is a first level problem that poses a challenge for Primary Care (PC). The overload of care in this area requires lower-cost and more accessible alternatives. Internet-based self-applied cognitive behavioral treatments (CBCT) have demonstrated their efficacy and added advantages. The "Smiling is fun" program has been validated in Spanish PC and has demonstrated its usefulness and cost-effectiveness. Previous studies have shown that professional support or guidance increases the results of the TCCI.
The aim of the present study is to contrast, by means of a randomized controlled trial, aims to examine the effectiveness, adherence rates, and implementation process of Smiling is Fun to address depression in a PC setting considering the influence of telephone support vs no support.
Ultimately, the results of the study could help in the uptake of sustainable resources so that the population could gain better access to psychological interventions in mental health services.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Rosa Lorente Català
- Phone Number: 0034 691527941
- Email: rlorente@uji.es
Study Locations
-
-
Valencia
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Tavernes de la Valldigna, Valencia, Spain, 46760
- Recruiting
- Psicología Clínica Unitat de Salut Mental Hospital Francesc de Borja
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Contact:
- Rosa Lorente Català
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age 18 to 65 years.
- Ability to understand and read Spanish.
- Meet diagnostic criteria for major depressive disorder (DSM-5).
- Mild or moderate symptoms of the Spanish version of the Beck Depression Inventory-II (BDI-II) (14-19: mild depression; 20-28: moderate depression).
- Episode duration of more than two weeks.
- Have internet access at home and an email account.
- The diagnosis of major depressive disorder will be confirmed by the standardized MINI International Neuropsychiatric Interview.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Professional support
Participants randomly assigned to this groups will receive the self-administered psychotherapy via the Internet a with telephone psychotherapeutic support.
|
Participants will receive an intervention called Smiling is Fun; a cognitve-conductual online program with the most effective psychological procedures for depression and other techniques to promote coping ability, emotional regulation and resilience along 8 modules. While they do the online program, they will receive periodically professional support. The professional support will be contacts of 20 minutes long, will take place every two weeks and will last 3 months. |
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Active Comparator: Non professional support
Participants randomly assigned to this group will receive the self-administered psychotherapy via the Internet without telephone psychotherapeutic support.
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Participants will receive an intervention called Smiling is Fun; a cognitve-conductual online program with the most effective psychological procedures for depression and other techniques to promote coping ability, emotional regulation and resilience along 8 modules.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Treatment efficacy
Time Frame: Pre-intervention, immediately after the intervention and follow-up (3,6 and 12 months).
|
Change of depression symtpmatology through the Beck Depression Inventory (BDI-II).
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Pre-intervention, immediately after the intervention and follow-up (3,6 and 12 months).
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quality of life related to health
Time Frame: Pre-intervention, immediately after the intervention and follow-up (3,6 and 12 months).
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The qualitiy of life related to health apsects will be measured using : EuroQol (EQ-5D) and Short Form Health Survey (SF-12)
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Pre-intervention, immediately after the intervention and follow-up (3,6 and 12 months).
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Adherence to the treatment
Time Frame: Immediately after the intervention
|
The adherence to the treatment will be assessed according to the moduls done by the patient in the plataform
|
Immediately after the intervention
|
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Implementation outcome: Feasibility
Time Frame: Immediately after the intervention
|
Professionals' assessment: Feasibility of Intervention Measure (FIM) (Weiner et al., 2017).
A four items scale on a 5-point Likert scale assess the feasibility of an intervention in a specific context.
The FIM showed high levels of internal consistency (α =0,89) and test-retest reliability coefficients (α =0,88).
|
Immediately after the intervention
|
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Implementation outcome: Acceptability
Time Frame: Immediately after the intervention
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Professionals' assessment: Acceptability of Intervention Measure (AIM) (Weiner et al., 2017).
A 4-item scale (from 1= completely disagree to 5= completely agree) that assesses the perception of the stakeholders about the agreeableness of treatment in a specific context.
The construct has shown good psychometric properties with high levels of internal consistency (α =0.89) and test-retest reliability (α =0.83).
|
Immediately after the intervention
|
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Implementation outcome: Appropiateness
Time Frame: Immediately after the intervention
|
Professionals' assessment: Intervention Appropriateness Measure (IAM) (Weiner et al., 2017).
A 4-item scale (from 1= completely disagree to 5= completely agree) that measures the appropriateness of the intervention.
The scale has shown good psychometric properties with high levels of internal consistency (α =0.87) and test-retest reliability (α =0.87)
|
Immediately after the intervention
|
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Implementation outcome: Normalization
Time Frame: Immediately after the intervention
|
Professionals' assessment: Normalization MeAsure Development Questionnaire (NoMAD) (Finch et al., 2018).
Based on the Normalization Process Theory, the NoMAD, a questionnaire of 13 items 5-Likert scale (from strongly agree to strongly disagree), has been developed to assess the process of normalization (May et al., 2009).
The NoMAD focuses on four dimensions: coherence, cognitive participation, collective action, and reflexive monitoring.
This questionnaire has demonstrated high levels of internal consistency along the four dimensions (20 items) (alpha=0.89).
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Immediately after the intervention
|
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Implementation outcome: Attitudes Towards Psychological Online Intervention
Time Frame: Immediately after the intervention
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Professionals' assessment: Attitudes towards Psychological Online Interventions (APOI) (Schröder et al., 2015).
A 16-item questionnaire, with a 5-point Likert scale, assesses attitudes toward IBT.
The APOI explores four dimensions; "Skepticism and Perception of Risks", "Confidence in Effectiveness", "Technologization Threat" and "Anonymity Benefits".
The scale has shown acceptable to good internal consistency (α=0.77)
(Schröder et al., 2015).
|
Immediately after the intervention
|
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Implementation outcome: Sustainability
Time Frame: Immediately after the intervention
|
Professionals' assessment: Barriers and facilitators of the implementation (FBI).
The FBI is a questionnaire specifically developed for this study and the study conducted by Lorente-Català et al. (2022).
The questionnaire was created following the systematic review on EBT implementation barriers and facilitators among third sector organizations (Bach-Mortensen et al., 2018).
As a result, 28 items assess the possible barriers, and 15 items evaluate the facilitators.
|
Immediately after the intervention
|
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Implementation outcome: Satisfactions
Time Frame: Immediately after the intervention
|
Client Satisfaction Questionnaire adapted to Internet-Based Interventions (CSQ-I; Boß et al., 2016).
This 9-item questionnaire assesses participants' satisfaction with IBI.
Items are presented on a 1 to 4 Likert scale in which 1 "does not apply to me" and 4 "does apply to me".
The total score ranges from 8 to 32.
It has adequate psychometric properties, Boß et al. (2016) rate Omega = 0.93 and 0.95 in two different samples.
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Immediately after the intervention
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Chair: Azucena García Palacios, Universidad Jaume I
- Study Director: Pedro Vera Albero, F.E.D. Psicología Clínica Unitat de Salut Mental Hospital Francesc de Borja
- Study Chair: Raquel Escriva Sanchis, F.E.D. Psicología Clínica Unitat de Salut Mental Hospital Francesc de Borja
- Study Chair: Clara Bretó García, F.E.D. Psicología Clínica Unitat de Salut Mental Hospital Francesc de Borja
Publications and helpful links
General Publications
- Mira A, Soler C, Alda M, Banos R, Castilla D, Castro A, Garcia-Campayo J, Garcia-Palacios A, Gili M, Hurtado M, Mayoral F, Montero-Marin J, Botella C. Exploring the Relationship Between the Acceptability of an Internet-Based Intervention for Depression in Primary Care and Clinical Outcomes: Secondary Analysis of a Randomized Controlled Trial. Front Psychiatry. 2019 May 10;10:325. doi: 10.3389/fpsyt.2019.00325. eCollection 2019.
- Romero-Sanchiz P, Nogueira-Arjona R, Garcia-Ruiz A, Luciano JV, Garcia Campayo J, Gili M, Botella C, Banos R, Castro A, Lopez-Del-Hoyo Y, Perez Ara MA, Modrego-Alarcon M, Mayoral Cleries F. Economic evaluation of a guided and unguided internet-based CBT intervention for major depression: Results from a multi-center, three-armed randomized controlled trial conducted in primary care. PLoS One. 2017 Feb 27;12(2):e0172741. doi: 10.1371/journal.pone.0172741. eCollection 2017.
- Montero-Marin J, Araya R, Perez-Yus MC, Mayoral F, Gili M, Botella C, Banos R, Castro A, Romero-Sanchiz P, Lopez-Del-Hoyo Y, Nogueira-Arjona R, Vives M, Riera A, Garcia-Campayo J. An Internet-Based Intervention for Depression in Primary Care in Spain: A Randomized Controlled Trial. J Med Internet Res. 2016 Aug 26;18(8):e231. doi: 10.2196/jmir.5695.
- Montero-Marin J, Prado-Abril J, Botella C, Mayoral-Cleries F, Banos R, Herrera-Mercadal P, Romero-Sanchiz P, Gili M, Castro A, Nogueira R, Garcia-Campayo J. Expectations among patients and health professionals regarding Web-based interventions for depression in primary care: a qualitative study. J Med Internet Res. 2015 Mar 10;17(3):e67. doi: 10.2196/jmir.3985.
- Karyotaki E, Riper H, Twisk J, Hoogendoorn A, Kleiboer A, Mira A, Mackinnon A, Meyer B, Botella C, Littlewood E, Andersson G, Christensen H, Klein JP, Schroder J, Breton-Lopez J, Scheider J, Griffiths K, Farrer L, Huibers MJ, Phillips R, Gilbody S, Moritz S, Berger T, Pop V, Spek V, Cuijpers P. Efficacy of Self-guided Internet-Based Cognitive Behavioral Therapy in the Treatment of Depressive Symptoms: A Meta-analysis of Individual Participant Data. JAMA Psychiatry. 2017 Apr 1;74(4):351-359. doi: 10.1001/jamapsychiatry.2017.0044.
- Mira A, Breton-Lopez J, Garcia-Palacios A, Quero S, Banos RM, Botella C. An Internet-based program for depressive symptoms using human and automated support: a randomized controlled trial. Neuropsychiatr Dis Treat. 2017 Mar 31;13:987-1006. doi: 10.2147/NDT.S130994. eCollection 2017.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- FISABIO
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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