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Interpersonal psychotherapy counseling for depressed children’s caregivers

Not Applicable
Conditions
Depression
F32.9
F01.145.126.350
Registration Number
RBR-5qhmb5
Lead Sponsor
niversidade Federal de São Paulo
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruitment completed
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

Depressive episode due to the presence of TDM according to the criteria of the DSMIVR received after administration of KSADS; score lower than 20 on the HDRS; both sex; be under 12 years old; parents must consent to participation by signing the informed consent form previously approved by the Ethics Committee of UNIFESP; preferably one caregiver to the child's mother with depressive episode due to TDM according to the DSMIVR criteria received after the SCIDI administration consent to the participation in the clinical trial.

Exclusion Criteria

Caregiver who receive treatment are using antidepressant medications or psychotherapy is in process; have a risk of suicide assessed by an item of PHQ9 scale, or have a score lower than 3 on the HAMD3, or through the clinical judgment of the SCID applicator; presents diagnostic criteria after administration of the SCIDI for psychoactive substances in the past 6 months; presents diagnostic criteria for bipolar disorder, schizophrenia or related disorders by administering the SCIDI; assumes that do not have the opportunity to follow the TIP sessions.

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Reduction or remission of depression symptoms from the entry, seen through the result of depression assessment tool in caregivers (Hamilton Rating Scale for Depression - HDRS) from the observation of the variation of at least 50% in depression scores pre and post intervention.
Secondary Outcome Measures
NameTimeMethod
Decrease of psychiatric and behavioral symptoms in children , assessed by CBCL (Check -list for behavioral and emotional problems ) from the observation on ths scores changes, from clinic range (>61)at pre-intervention to normal range (<60)at post-intervention.
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