Literature DB >> 17474807

Assessing the onset of antidepressant-induced sexual dysfunction using interactive voice response technology.

Judith A Dunn1, Renee Arakawa, John H Greist, Anita H Clayton.   

Abstract

BACKGROUND: Sexual dysfunction is a symptom of major depression, as well as a common complication of treatment with many classes of antidepressants. Nonetheless, the various forms of sexual dysfunction continue to be underreported in clinical practice, despite the availability of validated scales such as the Changes in Sexual Functioning Questionnaire (CSFQ). The current study was designed to evaluate the validity of obtaining CSFQ data using interactive voice response (IVR) technology.
METHOD: Sexually active, healthy male volunteers (N = 99; mean age of 31 years) were randomly assigned to 3 weeks of double-blind, parallel-group treatment with paroxetine (20 mg/day); CP-448,187 (3 mg/day); or placebo. Patients completed both paper-and-pencil and IVR versions of the 14-item CSFQ at baseline and on treatment days 8, 15, and 21. Additional IVR assessments were obtained at days 2, 4, and 6, permitting assessment of changes between office visits. This study was conducted between March and May 2001.
RESULTS: The overall correlation between the paper and IVR CSFQ total score was r = 0.96 (p < .0001). Similarly, high correlations were found between paper and IVR assessment methods on the individual CSFQ subscales: pleasure (r = 0.88), frequency (r = 0.88), interest (r = 0.93), arousal (r = 0.89), and orgasm (r = 0.92; p < .0001 for all comparisons). Both assessment methods were able to detect a statistically significant between-group difference in sexual functioning by day 8, which remained significant throughout the remainder of the study. Both assessment methods found SSRI-related sexual dysfunction to include significant effects on all CSFQ domains. Assessments using IVR collected from subjects at home on days 2, 4, and 6 identified onset of sexual dysfunction by day 4, before it was detected during scheduled office visits.
CONCLUSION: Interactive voice response assessment of sexual dysfunction on the CSFQ was found to be highly correlated with previously validated paper-and-pencil assessment. Interactive voice response provides a valid, easy-to-administer alternative method for obtaining systematic data on the impact of antidepressant treatment on sexual functioning. More frequent assessment by IVR enables more precise evaluation of symptom onset.

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Year:  2007        PMID: 17474807     DOI: 10.4088/jcp.v68n0406

Source DB:  PubMed          Journal:  J Clin Psychiatry        ISSN: 0160-6689            Impact factor:   4.384


  7 in total

1.  Neural correlates of antidepressant-related sexual dysfunction: a placebo-controlled fMRI study on healthy males under subchronic paroxetine and bupropion.

Authors:  Birgit Abler; Angela Seeringer; Antonie Hartmann; Georg Grön; Coraline Metzger; Martin Walter; Julia Stingl
Journal:  Neuropsychopharmacology       Date:  2011-05-04       Impact factor: 7.853

2.  Electronic versus paper diaries: a pilot study of concordance and adherence in head and neck cancer patients receiving radiation therapy.

Authors:  Joseph M Blondin; Khamis S Abu-Hasaballah; Howard Tennen; Rajesh V Lalla
Journal:  Head Neck Oncol       Date:  2010-10-18

3.  Evaluation of mode equivalence of the MSKCC Bowel Function Instrument, LASA Quality of Life, and Subjective Significance Questionnaire items administered by Web, interactive voice response system (IVRS), and paper.

Authors:  Antonia V Bennett; Kathleen Keenoy; Marwan Shouery; Ethan Basch; Larissa K Temple
Journal:  Qual Life Res       Date:  2015-11-21       Impact factor: 4.147

4.  Difference in method of administration did not significantly impact item response: an IRT-based analysis from the Patient-Reported Outcomes Measurement Information System (PROMIS) initiative.

Authors:  Jakob B Bjorner; Matthias Rose; Barbara Gandek; Arthur A Stone; Doerte U Junghaenel; John E Ware
Journal:  Qual Life Res       Date:  2013-07-23       Impact factor: 4.147

5.  Method of administration of PROMIS scales did not significantly impact score level, reliability, or validity.

Authors:  Jakob B Bjorner; Matthias Rose; Barbara Gandek; Arthur A Stone; Doerte U Junghaenel; John E Ware
Journal:  J Clin Epidemiol       Date:  2014-01       Impact factor: 6.437

6.  Mode equivalence and acceptability of tablet computer-, interactive voice response system-, and paper-based administration of the U.S. National Cancer Institute's Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE).

Authors:  Antonia V Bennett; Amylou C Dueck; Sandra A Mitchell; Tito R Mendoza; Bryce B Reeve; Thomas M Atkinson; Kathleen M Castro; Andrea Denicoff; Lauren J Rogak; Jay K Harness; James D Bearden; Donna Bryant; Robert D Siegel; Deborah Schrag; Ethan Basch
Journal:  Health Qual Life Outcomes       Date:  2016-02-19       Impact factor: 3.186

Review 7.  Equivalence of electronic and paper administration of patient-reported outcome measures: a systematic review and meta-analysis of studies conducted between 2007 and 2013.

Authors:  Willie Muehlhausen; Helen Doll; Nuz Quadri; Bethany Fordham; Paul O'Donohoe; Nijda Dogar; Diane J Wild
Journal:  Health Qual Life Outcomes       Date:  2015-10-07       Impact factor: 3.186

  7 in total

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