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N/A N=20 Randomized Single-blind Treatment

Neuropsychological Rehabilitation of Spontaneous Confabulation

Memory Disorders

Enrolled (actual)
20
Serious AEs
35.0%
Results posted
Mar 2016
Primary outcome: Primary: Number of Confabulations — 30.0; 29.9; 8.1; 35.5 Confabulations

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Neuropsychological treatment (Behavioral)
Age
Adult, Older Adult · 35+ yrs
Sex
All
Sponsor
Monica Triviño Mosquera
Primary completion
Apr 2015

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Confabulations
30.0; 29.9; 8.1; 35.5
PRIMARY
Number of Correct Responses
22.0; 20.9; 42.6; 22.0
PRIMARY
Number of Non-responses
26.3; 29.5; 22.3; 19.2
SECONDARY
Number of Errors in Source Attribution
25.1; 25.7; 12.2; 30.2

Summary

Confabulators consistently generate false memories without intention to deceive and with great feeling of rightness. However, there is currently no known effective treatment for them. In order to fill this gap, the aim of this trial was to design a neuropsychological treatment based on the current theoretical models and test it experimentally in two groups of confabulators: experimental vs. control. The treatment consisted of some brief material that patients had to learn and recall at both immediate and delayed moments. After both recollections, patients were given feedback about their performance (errors and correct responses). Pre-treatment and post-treatment baselines were administered. Confabulators in the control group performed the baselines without treatment, and were then offered the treatment after the second baseline.

Eligibility Criteria

Inclusion Criteria

  • The presence of spontaneous confabulations after acute brain injury, for at least three months and without clinical improvement (interfering with the patient's daily life with frequent arguments and exhaustive supervision).
  • The presence of momentary confabulations in the Spanish adaptation of Dalla Barba provoked confabulation interview.
  • Prior to injury, all patients should be completely independent for daily living.

Exclusion Criteria

  • The presence of impairment in alertness.
  • Dementia.
  • Acute confusional state.
  • A history of alcohol or drug abuse.
  • Psychiatric antecedents.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02540772). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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