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GRAU: Group-based therapy for anxiety reduction among university students

GRAU: Group-based interventions for the treatment of anxiety among university students with Acceptance and Commitment Therapy (ACT) and Cognitive Behavioral Therapy (CBT) - GRAU: GRAU: Grupos de intervenção para o tratamento da ansiedade em universitários

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-6wnw9t
Enrollment
Unknown
Registered
2020-02-11
Start date
2019-02-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Generalized anxiety disorder

Interventions

Three groups were performed, two intervention and one control group. One based on Acceptance and Commitment Therapy (ACT) which was composed of 10 members who participated in 12 group sessions held in
Behavioural

Sponsors

Universidade Federal do Rio Grande
Lead Sponsor
Universidade Federal do Rio Grande
Collaborator

Eligibility

Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion high anxiety. Moderate depression. No risk of suicide.

Exclusion criteria

Exclusion criteria: Exclusion Low level of anxiety.High level of depression. High risk of suicide.

Design outcomes

Primary

MeasureTime frame
The main outcome of this study will be the reduction on the levels of anxiety of participants. This outcome will be assessed through the instrument General Anxiety Disorder-7, translated and validated for use in Brazilian populations. This instrument consists of 7 questions about how the individual has been feeling in the last week. The questions are related to anxiety symptoms, with four possible answers, “rarely”, “few days”, “more than half days” and “almost every day”, scoring from 0 to 3, respectively. The difference on pré and post-intervention total score (ranging from 0 to 21) will be analyzed. Results will be tested through per protocol and intention-to-treat analysis.;There was a significant reduction in the mean level of anxiety in the intervention group between pre- and post-intervention assessments. On the other hand, there was no significant reduction in the mean level of anxiety in the control group between the pre-and post-intervention assessment. This treatment proved to be capable of reducing anxiety symptoms by 39.7% (mean score decreased from 15.125 to 9.125; p = 0.030) among patients who completed treatment (per protocol) and 30.8% (mean score decreased from 15 , 6 to 10.8; p = 0.035) among all allocated to the intervention group (ie, by intention to treat, including dropouts).

Secondary

MeasureTime frame
Secondary outcomes are not expected.;Secondary outcomes are not expected.

Countries

Brazil

Contacts

Public ContactRaimundo de Almeida

Universidade Federal do Rio Grande

raimundo.tkd@gmail.com555381601532

Outcome results

None listed

Source: REBEC (via WHO ICTRP)