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Effects of Cannabidiol on Burnout Syndrome and Empathy of Caregivers of Older Adults

U

University of Sao Paulo

Status and phase

Not yet enrolling
Early Phase 1

Conditions

Burnout Syndrome

Treatments

Drug: Intervention1: Cannabidiol
Drug: Intervention 2: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT06617247
79253324.5.0000.5440

Details and patient eligibility

About

Burnout syndrome is an occupational disease that has affected health care providers, for example, caregivers of older adults. This syndrome negatively affects physical and psychological health, which may reflect on the mental health of the caregiver and the care provided to the older adults. Interventions have been developed to minimize the impacts of burnout. Thus, this study has two main objectives: 1) to identify the effect of cannabidiol on indicators of burnout and empathy of caregivers of older people with functional dependence for activities of daily living; 2) identify possible associations between burnout indicators, empathy levels and their domains, and quality of care. This is a two-phase study (i.e., Phase 1: cross-sectional; Phase 2: clinical trial). In Phase 1, caregivers will answer questionnaires developed by researchers for sociodemographic characterization, care and satisfaction of care. In addition, they will complete instruments to assess the functional dependence of the older people - EIAVD, depressive symptoms - PHQ-9, social support - EAS, Burnout syndrome - MBI and Empathy - EMRI and MET. In Phase 2, caregivers will be randomized to cannabidiol or placebo intervention. Caregivers with number 0 will be allocated to the intervention using cannabidiol (300mg - divided into two times a day) and those drawn with number 1 will be allocated to the placebo group. Both interventions will be performed for four weeks. Caregivers will fill in the MBI, EMRI, MET, NPI and QAO instruments before and after the intervention. UKU-SERS will also be applied to evaluate side effects, IECC to assess the impact of intervention on care and CGI to assess severity and response to treatment.

Enrollment

26 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Total score 4 in the IEAVD
  • Score on the emotional exhaustion subscale of MBI 9 and/or depersonalization 6 and/or; professional achievement 10
  • Low level of empathy in the EMRI scale (i.e., total score 71)
  • In addition, they should have a score of 10 on the PHQ-9, indicating absence of expressive depressive symptoms

Exclusion criteria

  • Not have the availability to participate in this phase of the research will be excluded
  • Who have ceased to exercise the position of carer of a person aged 60 years or more
  • Who no longer perform minimum workload of six hours daily and
  • Not complete the protocol of the intervention received.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

26 participants in 2 patient groups

Intervention 2: Placebo
Experimental group
Description:
In this group, the subjects will receive placebo intervention. For blinding purposes, caregivers in this group will use the vehicle of oral CBD 300mg (150mg twice
Treatment:
Drug: Intervention 2: Placebo
Intervention1: Cannabidiol
Experimental group
Description:
The caregivers randomized for this intervention will use oral CBD 300 mg (i.e., 150mg, twice daily) for four weeks. The substance will be provided free of charge by the company Ease Labs, and will be administered in capsules to promote blinding. This posology was based on the study, in which CBD in this dosage and form of presentation proved to be safe and effective in reducing indicators of burnout in frontline health professionals from COVID-19. The safety of CBD use has also been reported in previous studies conducted with humans. Side effects from CBD use are rare, including mild and tolerable symptoms (e.g., dizziness, drowsiness, fatigue, lethargy, nausea, headache, fever, and sensory changes).
Treatment:
Drug: Intervention1: Cannabidiol

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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