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A Randomised Controlled Clinical Trial of Memory Specificity Training (MEST) for Depression

U

United Kingdom Research and Innovation (UKRI)

Status

Completed

Conditions

Depressive Symptoms
Major Depressive Disorder

Treatments

Behavioral: Education and Support
Behavioral: Memory Specificity Training

Study type

Interventional

Funder types

Other

Identifiers

NCT01882452
MEST-UK

Details and patient eligibility

About

Depression involves the tendency to recall overgeneral personal memories, a phenomenon which has been linked to numerous adverse psychological outcomes. The purpose of this study is to investigate whether a group-based Memory Specificity Training (MEST) programme improves outcomes in depression, and how this compares to an education and support control group. The primary aim is to examine whether MEST, which involves repeated practice retrieving specific autobiographical memories reduces depressive symptoms immediately post-treatment, and whether this is maintained 3 months after treatment. The secondary objective of this trial is to examine the role of hypothesised cognitive processes (ie., rumination, executive control, cognitive avoidance) which may underlie improvements in depression and memory.

Enrollment

60 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Principal diagnosis of Major Depressive Disorder
  • History of more than one previous depressive episode
  • Current diagnosis of a Major Depressive Episode
  • Depressive symptoms rated in the mild-severe range (> 13 on the BDI-II)
  • Memory specificity < .70 (as assessed on the AMT)

Exclusion criteria

  • Head trauma
  • Organic brain damage
  • Secondary diagnosis of another affective disorder
  • Psychosis
  • Current drug or alcohol abuse or dependence
  • A diagnosed Axis II disorder

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Memory Specificity Training
Experimental group
Description:
Five weekly one-hour sessions of memory specificity training administered in groups of 5-8 participants.
Treatment:
Behavioral: Memory Specificity Training
Education and Support
Active Comparator group
Description:
Five weekly one-hour sessions of an education-and-discussion supportive intervention, administered in groups of 5-8 participants.
Treatment:
Behavioral: Education and Support

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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