ClinicalTrials.Veeva

Menu

Neuropsychological Rehabilitation of Spontaneous Confabulation: a Replica Study

M

Monica Triviño Mosquera

Status

Completed

Conditions

Memory Disorders

Treatments

Behavioral: Neuropsychological treatment

Study type

Interventional

Funder types

Other

Identifiers

NCT03183453
Conf-02

Details and patient eligibility

About

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, we performed a neuropsychological treatment in two groups of confabulators: experimental vs. control (ClinicalTrials.gov ID: NCT02540772).

Now, we intend to replicate the treatment with a larger sample of confabulators and with other two control groups: non-confabulator patients with brain injury and healthy individuals

Full description

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 measurements were administered.

Non-confabulator patients and healthy participants performed only the pre-treatment measurement.

Enrollment

57 patients

Sex

All

Ages

35 to 80 years old

Volunteers

Accepts Healthy Volunteers

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 drug abuse.
  • Psychiatric antecedents.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

57 participants in 3 patient groups

Neuropsychological treatment
Experimental group
Description:
The tested treatment is a combination of neuropsychological rehabilitation procedures: learning, episodic memory recall after a delay, selective attention, inhibition of predominant responses and awareness of deficits.
Treatment:
Behavioral: Neuropsychological treatment
Non-confabulators control group
No Intervention group
Description:
Non-confabulators (brain injured patients but without confabulations) in this control group only performed the pre- and post-measurements without treatment.
Healthy control group
No Intervention group
Description:
Healthy participants in this control group only performed the pre- and post-measurements without treatment.

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems