Memory Rehabilitation by Means of Working Memory Training in Combination With a Recollection Training
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ClinicalTrials.gov Identifier: NCT02790151 |
Recruitment Status :
Completed
First Posted : June 3, 2016
Last Update Posted : October 18, 2016
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Memory Deficits | Behavioral: Standard Therapy Behavioral: Experimental Intervention | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 36 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Double (Participant, Investigator) |
Primary Purpose: | Treatment |
Official Title: | Memory Rehabilitation by Means of Working Memory Training in Combination |
Study Start Date : | November 2014 |
Actual Primary Completion Date : | October 2016 |
Actual Study Completion Date : | October 2016 |

Arm | Intervention/treatment |
---|---|
Active Comparator: Standard Therapy
Learning and practicing memory strategies
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Behavioral: Standard Therapy
Learning and practicing Memory strategies |
Experimental: Experimental Intervention
Computerbased working memory training and Recollection training
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Behavioral: Experimental Intervention
Computerbased Working Memory Training in Combination with a Recollection Training |
- Test to assess change in memory performance in everyday life [ Time Frame: baseline and 9 hours ]The test includes different single tasks that measure memory in everyday life e.g. Story recall (Subtest 6 from the Rivermead Behavioral Memory Test) Outcome measure: Total number of points
- Outcome change in different neuropsychological tests [ Time Frame: baseline and 9 hours ]Tests for verbal memory, working memory, prospective memory, attention and word fluency (Composite scores built from raw scores)

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Ages Eligible for Study: | Child, Adult, Older Adult |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- brain injury
- memory deficits (performance below average in the California Verbal Learning Test in learning trial 1 or 5, sfr or lfr)
Exclusion Criteria:
- severe amnesia (less than 2 words in sfr of the CVLT), dementia, sensory or motor aphasia, impaired vision, insufficient German language skills, lack of patient's consent

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02790151
Germany | |
Rehabilitationszentrum GmbH | |
Oldenburg, Deutschland, Germany, 26131 |
Study Director: | Helmut Hildebrandt, Prof. Dr. | Universität Oldenburg |
Responsible Party: | Kim Merle Richter, MSc Psychologie, University of Oldenburg |
ClinicalTrials.gov Identifier: | NCT02790151 |
Other Study ID Numbers: |
UOLDENBURG |
First Posted: | June 3, 2016 Key Record Dates |
Last Update Posted: | October 18, 2016 |
Last Verified: | October 2016 |
working memory, recollection training, transfer |
Memory Disorders Neurobehavioral Manifestations Neurologic Manifestations Nervous System Diseases |