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Effectiveness of an alternative intervention in the treatment of depressive symptoms.

Journal of affective disorders
January 1, 1970
Leandro Cardozo-Batista et al. (2 authors)
Journal ArticleRandomized Controlled TrialResearch Support, Non-U.S. Gov'tHuman StudyClinical
Study Details

Study Goal

The researchers aimed to test a natural therapy protocol, including Mindfulness Meditation, as an alternative to pharmacological and psychotherapeutic treatments for reducing depression symptoms in individuals not receiving traditional treatment.

Results Summary

The study found a significant reduction in depression symptoms in the experimental group after the intervention, though it could not determine which specific technique was most effective.

Population

Individuals with depression symptoms not receiving pharmacological or psychotherapeutic treatment (n=21).

Effective Dosage

Not specified (eight sessions over two months).

Duration

Two months.

Interactions

None mentioned.

Extracted Claims (1)
InterventionDirectionEndpointPopulationDosageImpactClaim #
protocol based on natural therapy, alternatives to pharmacological and psychotherapeutic, through Mindfulness Meditation, Reiki, Acupuncture and Auriculotherapy
decrease
symptoms of depression
participants who were with no pharmacological or psychotherapeutic treatment for these symptoms
-
significant reduction
#1
Abstract

BACKGROUND: There is a scarcity of studies in the international literature regarding alternative treatment to the pharmacological and psychotherapeutic intervention in the face of depression symptoms. This study aimed to test a protocol based on natural therapy, alternatives to pharmacological and psychotherapeutic, through Mindfulness Meditation, Reiki, Acupuncture and Auriculotherapy, to treat the symptoms of depression for those who were with no pharmacological or psychotherapeutic treatment for these symptoms. METHODS: this is a randomized single-blind controlled pilot study. The final sample was 21 participants divided in two groups: experimental and control. Participants were evaluated by validated instruments during the screening process and after the intervention. The instruments were: Depression, Anxiety and Stress Scale and Beck Depression Inventory. Intervention was performed in eight sessions, during two months. All the techniques were used in the experimental group. Analysis of variance with repeated measures was used to compare pre-intervention to post-intervention moments. RESULTS: the result of analysis indicates a significant reduction in the symptoms of depression after the intervention among the experimental group. LIMITATIONS: there is no way to determine which of the techniques used produced the most significant result. CONCLUSIONS: The protocol proposed in this study was effective in reducing the symptoms of depression to whom are not eligible for traditional treatment.

Medical Subject Headings (MeSH)
AnxietyAnxiety DisordersDepressionHumansMeditationMindfulnessSingle-Blind Method
Study Links
Quality Scores
SafetyNot Assessed
Efficacy85/10
Quality70/10
Citation Metrics
Total Citations6
Citations/Year1.2
Relative Citation Ratio0.89
NIH Percentile45.8%
Research Impact Scores
APT Score0.50
Weight Score1.47
Normalized Score0.68
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