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Brief Cognitive Behavioral Therapy Versus Crisis Intervention Therapy Through Telepsychiatry on Psychiatric Symptoms

U

Universidad Nacional Autonoma de Honduras

Status

Unknown

Conditions

Depressive Symptoms
Post Traumatic Stress Symptoms
Anxiety
Perceived Stress

Treatments

Behavioral: Brief cognitive behavioral therapy
Behavioral: Crisis intervention therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT04394455
1503202018052020242912

Details and patient eligibility

About

The purpose of this randomized controlled trial is to determine the effect of two behavioral interventions: brief cognitive-behavioral therapy and crisis intervention therapy through telepsychiatry, over the level of perceived stress, anxiety, depression and post-traumatic stress symptoms during the COVID-19 pandemic in medical residents and medical staff at three hospitals in two cities of Honduras.

Full description

The psychotherapeutic interventions are going to be delivered from June to August at each participating center. Subjects will be allocated randomly in each of the two interventional arms independently by stratification in each participating center. The population for intervention will be medical staff from three different national hospitals in the frontline during the pandemic. After valid informed consent, a screening process will take place to identify symptoms as baseline evaluation using validated self-assessment tools delivered through electronic invitation. Post-intervention measurements will take place at 3 and 6 months from baseline. Intention to treat analysis and per-protocol analysis will take place. CONSORT guidelines were followed.

Enrollment

236 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Medical doctors and medical residents 18 years and older, from UNAH medical school and Hospital de Occidente.
  • Medical doctors and medical residents whom during the initial screening show positive scores in Patient Health Questionnaire-2 and Generalized Anxiety Disorder scale-2
  • Access to internet and an electronic device

Exclusion criteria

  • Medical doctors and medical residents referring a history of psychiatric disorders
  • Medical residents that belong to the Psychiatry Residency Program
  • Medical residents and medical doctors that have been diagnosed with COVID-19
  • Medical doctors and residents whom during evaluations show severe symptoms of depression, anxiety and post-traumatic stress symptoms
  • Medical doctors and residents with negative screening in Patient Health Questionnaire-2 and Generalized Anxiety Disorder Scale-2
  • Participants that do not have access to internet connection or an electronic device.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

236 participants in 2 patient groups

Brief cognitive behavioral therapy
Experimental group
Description:
Medical staff (medical doctors and residents) who will receive brief cognitive behavioral therapy through telepsychiatry.
Treatment:
Behavioral: Brief cognitive behavioral therapy
Crisis intervention therapy
Active Comparator group
Description:
Medical staff (medical doctors and residents) who will receive 3 sessions of crisis intervention therapy through telepsychiatry.
Treatment:
Behavioral: Crisis intervention therapy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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