Testing Effect and Schizophrenia

December 15, 2025 updated by: University Hospital, Strasbourg, France

Retrieval Practice in Patients With Schizophrenia : an Exploratory Study Using Word Pairs

When people are tested on a previously learned material, they will latter remember it better even when compared to a condition where they can re-study it. This phenomenon is called retrieval practice and is supported by an extensive research literature mostly carried out in normal students. This paradigm begins to be used in cognitive remediation programs in patients suffering from memory difficulties.

The objective of this study is to investigate whether retrieval practice is spared in patients with schizophrenia.

If effective, this method could be used in cognitive remediation programs.

Since episodic memory difficulties are supposed to be secondary to deficits in the initiation/elaboration of efficient encoding and retrieval strategies our hypothesis is that retrieval practice is spared in schizophrenia

Study Overview

Study Type

Interventional

Enrollment (Actual)

40

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Laxou, France, 54521
        • Centre Psychothérapique de Nancy
      • Strasbourg, France, 67091 Cedex
        • Service de psychiatrie - Hôpital Civil - CHRU Strasbourg

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 60 years (Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • French is the native language, or acquired before 5 years old
  • People must be able to understand and follow the trial instructions

Specific inclusion criteria (for patients) :

  • Diagnostic of schizophrenia, according to the DSM -5, clinically stable
  • The treatment must remain unchanged during the trial

Exclusion Criteria:

  • Severe or acute cerebral disease
  • Other actual psychiatric disorder
  • Use of drugs with high anticholinergic effect
  • Irregular use of benzodiazepines medication, or high dose of benzodiazepin (more than 2 mg of lorazepam per day or equivalent)
  • Inappropriate use of drugs

Specific exclusion criteria (for healthy subjects) :

- Diagnostic of schizophrenia of a relative up to the third degree

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Healthy subjects

In the first phase (encoding), people study a list of 48 word pairs non semantically associated.

Then (initial test), they recall half of word pairs or restudy the other half.

In the second phase (final test) which takes place 2 days later, they recall all the 48 the word pairs.

Experimental: Patients with schizophrenia

In the first phase (encoding), people study a list of 48 word pairs non semantically associated.

Then (initial test), they recall half of word pairs or restudy the other half.

In the second phase (final test) which takes place 2 days later, they recall all the 48 the word pairs.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of word pairs properly recalled
Time Frame: Final test : 2 days after the first experimental session

- The aim is to investigate the retrieval practice effect using word pairs and cued recall tests with feedback in patients with schizophrenia and healthy controls.

In the first phase (encoding), people study a list of 48 word pairs non semantically associated, then half of the pairs are presented in its completed form for two times, and for the other half the two subsequent re-exposure trials are framed as cued recall tests (the first word is presented and the subject has to remember and give orally the second word, and a feedback is given).

In the second phase (final test) which takes place 2 days later, all the 48 word pairs are presented as a cued recall test.

- We will compare in patients with schizophrenia and healthy controls final performance recall for information studied and recalled ("test" condition) to those for information studied and then re-studied ("re-study" condition).

Final test : 2 days after the first experimental session

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Difference between final performance recall and memory span score
Time Frame: Final test : 2 days after the first experimental session

In each group (patients with schizophrenia and healthy controls) :

Difference between the final performance recall (see primary outcome measure) in "test" condition and "re-study" condition AND memory span score.

Final test : 2 days after the first experimental session

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 1, 2014

Primary Completion (Actual)

May 6, 2015

Study Completion (Actual)

August 1, 2015

Study Registration Dates

First Submitted

May 26, 2014

First Submitted That Met QC Criteria

May 26, 2014

First Posted (Estimated)

May 29, 2014

Study Record Updates

Last Update Posted (Estimated)

December 22, 2025

Last Update Submitted That Met QC Criteria

December 15, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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