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Management of Psychological and Behavioral Symptoms in Patients With Dementias (PRESTA)

P

Pere Virgili Health Research Institute (IISPV)

Status

Completed

Conditions

Family Relations
Psychological and Behavioral Symptoms
Dementia

Treatments

Other: Educational therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT03732521
CEIC-10/2014

Details and patient eligibility

About

Background: The psychological and behavioral symptoms (SPCD) of dementias are the manifestations that cause the most suffering in the patient and caregiver, worsening the other two symptomatic areas (cognitive and functional) and precipitating the early institutionalization of patients with dementia. non-pharmacological therapies (TNF) in dementia are framed in the biopsychosocial model of patient care. We found evidence in the literature about the effectiveness of ambulatory educational interventions to the family caregiver in terms of reducing overload and improving their state of mind But it is not well demonstrated whether this improvement can have an indirect impact on the SPCD of the patient, nor whether the profile of patients could have an added benefit to the best pharmacological treatment.

Methods: The experimental study selected thirty-six older adults family caregivers of patients with dementia.The intervention group (n=18) received isolated medical treatment, while the control group (n=18) received medical treatment plus educational support therapy to their family caregivers. Data collection included sociodemographic measures and responses to the educational support therapy tot the Zarit Caregiver Overload Scale (family caregivers) and Neuropsychiatric Inventory (NPI-10) patients with dementia.

Full description

A descriptive analysis of the sociodemographic characteristics of the intervention and control groups was done. Qualitative variables were expressed as percentages, and quantitative variables were summarised as the median and interquartile range.

Shapiro-Wilk tests indicated that the dependent variables were not normally distributed (p < .05), so non-parametric statistical analyses were subsequently performed. The difference between the medians of the two patient groups was examined with the Mann-Whitney U test. Qualitative variables were compared with the chi-squared or Fisher's exact test, as appropriate.

Enrollment

36 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of at least 6 months of dementia and on treatment with IACEs ± memantine.
  • Patients diagnosed with dementia, who score on the global scale of Severity of Reisberg between 4 and 6, both included.
  • Patients who at least obtain a score ≥ 4 on the NPI scale, version validated in Spanish. The symptoms must be present at least one month prior to the visit and will not be attributable to intercurrent medical pathology or to acute confusional syndrome.
  • Patients living in a family home, and accompanied by a family caregiver who agrees to sign the informed consent after obtaining all the information of the study in question.

Exclusion criteria

  • Patients with a diagnosis of mild cognitive impairment or who do not take specific medication (IACEs and / or memantine).
  • Patients with severe sensory deprivation that does not allow MMSE scale assessment.
  • Patients who present intercurrent medical illnesses that confers a poor short-term vital prognosis (6 months).
  • Patients in which the SPCD may be in the context of a toxicometabolic disease, uncontrolled pain or delirium, according to the researcher's clinical criteria.
  • Patients who are taking typical neuroleptics, long-acting BZD, major opioids or drugs that can potentially alter the state of consciousness.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

36 participants in 2 patient groups

Intervention group
Experimental group
Description:
educational therapy
Treatment:
Other: Educational therapy
Control group
No Intervention group
Description:
usual clinical practice

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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