Self-Reported Depressive Symptom Measures: Sensitivity to Detecting Change in a Randomized, Controlled Trial of Chronically Depressed, Nonpsychotic Outpatients: Clinical Research
This study evaluated and compared the performance of three self-report measures: (1) 30-item Inventory of Depressive Symptomatology-Self-Report (IDS-SR 30 ); (2) 16-item Quick Inventory of Depressive Symptomatology-Self-Report (QIDS-SR 16 ); and (3) Patient Global Impression-Improvement (PGI-I) in a...
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Veröffentlicht in: | Neuropsychopharmacology (New York, N.Y.) N.Y.), 2005-02, Vol.30 (2), p.405-416 |
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Zusammenfassung: | This study evaluated and compared the performance of three self-report measures: (1) 30-item Inventory of Depressive Symptomatology-Self-Report (IDS-SR
30
); (2) 16-item Quick Inventory of Depressive Symptomatology-Self-Report (QIDS-SR
16
); and (3) Patient Global Impression-Improvement (PGI-I) in assessing clinical outcomes in depressed patients during a 12-week, acute phase, randomized, controlled trial comparing nefazodone, cognitive-behavioral analysis system of psychotherapy (CBASP), and the combination in the treatment of chronic depression. The IDS-SR
30
, QIDS-SR
16
, PGI-I, and the 24-item Hamilton Depression Rating Scale (HDRS
24
) ratings were collected at baseline and at weeks 1–4, 6, 8, 10, and 12. Response was defined
a priori
as a ⩾50% reduction in baseline total score for the IDS-SR
30
or for the QIDS-SR
16
or as a PGI-I score of 1 or 2 at exit. Overall response rates (LOCF) to nefazodone were 41% (IDS-SR
30
), 45% (QIDS-SR
16
), 53% (PCI-I), and 47% (HDRS
17
). For CBASP, response rates were 41% (IDS-SR
30
), 45% (QIDS-SR
16
), 48% (PGI-I), and 46% (HDRS
17
). For the combination, response rates were 68% (IDS-SR
30
and QIDS-SR
16
), 73% (PGI-I), and 76% (HDRS
17
). Similarly, remission rates were comparable for nefazodone (IDS-SR
30
=32%, QIDS-SR
16
=28%, PGI-I=22%, HDRS
17
=30%), for CBASP (IDS-SR
30
=32%, QIDS-SR
16
=30%, PGI-I=21%, HDRS
17
=32%), and for the combination (IDS-SR
30
=52%, QIDS-SR
16
=50%, PGI-I=25%, HDRS
17
=49%). Both the IDS-SR
30
and QIDS-SR
16
closely mirrored and confirmed findings based on the HDRS
24
. These findings raise the possibility that these two self-reports could provide cost- and time-efficient substitutes for clinician ratings in treatment trials of outpatients with nonpsychotic MDD without cognitive impairment. Global patient ratings such as the PGI-I, as opposed to specific item-based ratings, provide less valid findings. |
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ISSN: | 0893-133X 1740-634X |
DOI: | 10.1038/sj.npp.1300614 |