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Efficacy of an Online Program for the Treatment of Mild and Moderate Depression

Efficacy the Online Program iFightDepression for the Treatment of Mild and Moderate Depression

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02312583
Enrollment
310
Registered
2014-12-09
Start date
2015-01-31
Completion date
2018-12-31
Last updated
2016-10-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression

Keywords

depression, cognitive-behavior intervention

Brief summary

iFighDepression is an online self-help programme based on cognitive-behavioral therapy that could be useful for the treatment of mild to moderate depression

Detailed description

Major depression (MD) is a disease with a great impact on people´s functioning and is the second leading cause of disability worldwide. It is a condition with a high prevalence, about 10% of men and 20% of women in the population will be diagnosed MD throughout their lives, and has an effect on high economic costs to health services. While there are many effective therapeutic options for the treatment of depression, many people with depressive episodes do not receive an appropriate treatment or, in fact, do not receive any treatment at all. The social stigma, difficulties to access mental health services, to integrate therapy sessions into working life, or problems to pay for treatment are some of the main barriers to receive adequate treatment. On-line interventions are easily accessible and low cost, and different studies suggest that these interventions have significant and lasting improvements in different mental disorders. These studies indicate that this type of treatment would be indicated for disorders that, as the case of MD, have a high prevalence and relatively low help-seeking for treatment. iFighDepression is an online self-help programme for mild to moderate depression that has been developed in the context of the European project Preventing Depression and Improving Awareness through Networking in the European Union (PREDI-NU) which is managed by the European Alliance Against Depression (EAAD). It involves the most complete integration of the cognitive-behavioral online programs available to date, which is a format of intervention that has been proven effective in reducing depressive symptoms in several randomized controlled trials. IFightDepression is currently in pilot phase in 7 European Union countries, including Spain. The purpose of this project is to study the therapeutic effect of the iFightDepression online programme in patients with mild to moderate depression

Interventions

BEHAVIORALPsychoeducational online information

Psychoeducational online information. During 7 weeks as a complement to the usual treatment. Participants will have access to online psychoeducational material for depression.

BEHAVIORALiFightDepression online programme

iFightDepression online programme. During 7 weeks as a complement to the usual treatment. Participants will complete the modules of a structured online programme for depression

Sponsors

Instituto de Salud Carlos III
CollaboratorOTHER_GOV
Parc de Salut Mar
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosis of major depressive disorder according to Diagnostic and Statistical Manual (DSM-IV-TR) criteria. * Clinical severity between mild and moderate (according to ICG severity scale). * A minimum of reading comprehension and knowledge of internet browsing. * Availability to access internet during the 7 weeks of the intervention. * Informed written consent provided.

Exclusion criteria

* Suicidal ideation (assessed by the HDRS and clinical interview). * Presence of delusional ideas or hallucinations, consistent or not with the mood. * Other concomitant psychiatric pathologies of the Axis I or Axis II according to Diagnostic and Statistical Manual (DSM-IV-TR) at the time of entry to the study. * To be currently enrolled in a structured programme/treatment of psychotherapy.

Design outcomes

Primary

MeasureTime frameDescription
Change in depression ScaleFrom baseline to 7 weeksEfficacy will be assessed by using the Hamilton Depression Scale, version 17 items (HDRS-17). The HDRS-17 will be administered at baseline, 4 weeks and 7 weeks.

Secondary

MeasureTime frameDescription
Change in depressive symptomatologyFrom baseline to 7 weeksDepressive symptomatology measured by the Self-Report Patient Health Questionnaire-9 (PHQ-9). Measure will be done once a week.
Change in the Remission from DepressionFrom baseline to 7 weeksRemission from Depression Questionnaire (RDQ): Self-Report in relation to different domains considered as relevant by the patients themselves in defining the construct of remission in the scope of depressive disorders. Measure will be done once a week.
Change in the Clinical Global Impression of Severity and ImprovementFrom baseline to 7 weeksClinical Severity will be assessed using the Scale of Clinical Global Impression of Severity and Improvement (ICG-s and ICG-m). Hetero and Self-Administered versions. Scale of Clinical Global Impression of Severity and Improvement (ICG-s) at baseline. and at 7 weeks Scale of Clinical Global Impression of Severity and Improvement (ICG-m) at baseline and at 7 weeks.
Change in functional impairmentFrom baseline to 7 weeksFunctional impairment assessed by using the Functioning Assessment Short Test (FAST). It evaluates the functional impairment in patients suffering from mental illness, including the Major Depression.
Users satisfaction scoreOne measure at 7 weeksUser´s satisfaction by using the Satisfaction Questionnaire: a questionnaire of satisfaction used in the validation of the programme iFightDepression within the project PREDI-NU. It includes questions about the manageability of the programme and the beneficial aspects perceived by the user.
Change in quality of lifeFrom baseline to 7 weeksChange measured using the EuroQoL Quality of Life Scale (EQ-5 d). It is a Self-Report measure of health variables which is commonly used as an indicator of quality of life.

Countries

Spain

Contacts

Primary ContactVictor Perez, MD, PhD
VPerezSola@parcdesalutmar.cat+34932483495
Backup ContactAzucena Justicia, RMN, MSc
ajusticia@imim.es+34932483495

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026