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NCT01007682 · ClinicalTrials.gov registry record · NA

Intrusive Reexperiencing: The Role of Working Memory Capacity and Thought Suppression

A NA study, sponsored by University Hospital, Basel, Switzerland.

Completed
Registry status
NA
Development phase
200
Enrollment target

NCT01007682 is a NA study that has completed, run by University Hospital, Basel, Switzerland. The registered enrollment target is 200 participants.

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The verdict

NCT01007682, a NA study, has completed, sponsored by University Hospital, Basel, Switzerland.

COMPLETED
Registry status
NA
Development phase
200 participants
Enrollment target

Study Summary

This study aims at identifying risk factors for the development of intrusive reexperiencing symptoms. In particular, the investigators examine the influence of working memory capacity and thought suppression on the occurrence of unpleasant memories of a negative experience. Hypothesis: People with high working memory capacities (HWMC) are able to successfully suppress memories of an unpleasant experience (presentation of a distressing movie). In contrast, in people with low working memory capacities (LWMC), attempts to suppress memories of an unpleasant experience inadvertently lead to an increase of these memories. Study phase one: Assessment of working memory capacity in 200 healthy participants by means of a computerized task. Selection of 50 participants with HWMC and of 50 participants with LWMC who participate in study phase two. Study phase two: Presentation of a distressing movie and subsequent assessment of memories of the movie during several days in the daily life of participants. Comparison of 4 groups regarding the frequency of instructions in daily life:(group 1: HWMC participants who are instructed to suppress thoughts of the movie, group 2: LWMC participants who are instructed to suppress thoughts of the movie, group 3: HWMC participants who are instructed to allow the occurence of thoughts of the movie, group 4: LWMC participants who are instructed to allow the occurence of thoughts of the movie)

Interventions

  • OTHER Show distressing movie and tell half of the two study groups to suppress memories of the movie

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2009-09
Est. Completion 2011-10
Phase NA

What the Registry Record Tells You About NCT01007682

The ClinicalTrials.gov registry entry for NCT01007682 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University Hospital, Basel, Switzerland, which has 12 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Show distressing movie and tell half of the two study groups to suppress memories of the movie is the first listed.

NCT01007682 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01007682 about?

NCT01007682 is a clinical study titled "Intrusive Reexperiencing: The Role of Working Memory Capacity and Thought Suppression". This study aims at identifying risk factors for the development of intrusive reexperiencing symptoms. In particular, the investigators examine the influence of working memory capacity and thought suppression on the occurrence of unpleasant memories of a negative experience. Hypothesis: People with ...

What is the current status of trial NCT01007682?

This trial is currently completed. It is a NA study. The enrollment target is 200 participants. The study started on 2009-09. Estimated completion is 2011-10.

What interventions are being tested in trial NCT01007682?

The interventions under investigation include: Show distressing movie and tell half of the two study groups to suppress memories of the movie (OTHER).

Who is sponsoring clinical trial NCT01007682?

This trial is sponsored by University Hospital, Basel, Switzerland, which has 12 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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