The use of a Therapeutic Tool to reduce symptoms of Depressio

Not Applicable

• Conditions: Depression; depressive disorder; F01.145.126.350; F03.600.300

• Registration Number: RBR-5prgcn
• Lead Sponsor: niversidade Federal de Alagoas

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-05-07
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Data analysis completed
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

18 years of age or older; being accompanied in the service due to depression; being on medication for depression; meet the criteria of the International Neuropsychiatric Interview (MINI) for depression; present scores from 20 to 63 of the Beck Depression Inventory (BDI)

Exclusion Criteria

Persons in acute stage of hallucination and dissociation; in dependence on psychoactive substances, except nicotine

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Expected outcome 3: Improvement in hopelessness rating, assessed by the Beck Hopelessness Scale, from the observation of a variation of at least 5% in the pre and post-intervention measurements;Expected outcome 4: Improvement in anxiety rating, assessed by the Beck Anxiety Inventory, from the observation of a variation of at least 5% in the pre and post-intervention measurements;Expected outcome 2: Reduction of suicide risk, evaluated by the Suicidal ideation scale, from the observation of a variation of at least 5% in the pre and post-intervention measurements ;Expected outcome 1: Reduction of depressive symptoms, evaluated by the Beck Depression Inventory, from the observation of a variation of at least 5% in the pre and post-intervention measurements

Secondary Outcome Measures

Name	Time	Method
Secondary outcomes are not expected