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OpenTrials
Completed

NCT Number: NCT00202462

The Effect of Testosterone on Mood and Quality of Life

We hypothesize that testosterone replacement will improve mood and quality of life in older men with low testosterone and mild depression. Study subjects will receive either testosterone gel or a placebo (inactive) gel for 12 weeks. Neither the subject or the investigator will know whether they are receiving placebo or testosterone gel. At the end of the initial 12 week period, all subjects will receive testosterone gel for 12 more weeks. Mood and quality of life measures will be obtained at baseline, at the end of the double-blind phase and at the end of the extension phase (when all subjects receive testosterone.)

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Key information

Age range

50 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

About this study

This is a randomized, double-blind, placebo-controlled trial of testosterone replacement in older men with age-associated hypogonadism and subsyndromal depression. Men will receive either 7.5 gm/qd of testosterone gel or a placebo gel for 12 weeks. The double-blind phase will be followed by a 12 week open-label extension in which all subjects will receive 7.5 gm/qd of testosterone gel.

Procedures: Depressive symptoms will be assessed with the Hamilton Depression Rating Scale (HDRS) and the SCL-20, a 20-item self-report depression scale that has been shown to have high reliability and validity and to be sensitive to changes in depressive symptoms in outpatients in primary care settings. The short form (16 item) Endicott Quality of Life Enjoyment and Satisfaction Scale will be used to assess quality of life changes. The Medical Outcomes Study Short-Form 36 (SF-36) will be used to assess changes in functional status. Demographic information, medical history and current medications will be determined at baseline and follow up, via patient interview and chart review. Overall medical morbidity will be ascertained with the Cumulative Illness Rating Scale. All outcome measures (SCL-20, Endicott Quality of Life Scale, HDRS,SF-36) will be assessed at baseline, week 12 (end of the double-blind phase)and week 24 (end of the extension phase). Blood draws will be done at baseline, week 12 and week 24. Laboratory assays for testosterone leves at baseline, week 12 and week 24 will be performed at the same time to minimize interassay variability.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age: 50 or older
  • Total Testosterone <=280 ng/dl
  • Subsyndromal depressive disorder: either dysthymia or minor depression (per DSM IV and DSM IV appendix)

Exclusion criteria

  • PSA >=3.0
  • Klinefelter's syndrome
  • Prostate or breast cancer
  • Hospitalized in the past month
  • Obstructive BPH
  • Current testosterone treatment
  • Schizophrenia, bipolar disorder, dementia
  • Treatment with antipsychotics or benzodiazepines
  • Alcohol dependence or other substance dependence
  • Suicidal or psychotic symptoms

Treatment and study plan

Testosterone gel

Drug

Testosterone gel 7.5 gm qd

Other names: Androgel

Primary outcomes

  1. Hamilton Depression Rating Scale

    Time frame: 12 and 24 weeks

Secondary outcomes

  1. SF-36

    Time frame: 12 and 24 weeks

  2. Endicott Short Quality of Life Scale

    Time frame: 12 and 24 weeks

  3. SCL-20

    Time frame: 12 and 24 weeks

Sponsors and collaborators

Lead sponsor

Seattle Institute for Biomedical and Clinical Research

Other

Collaborators

  • American Federation for Aging Research
  • Geriatric Research Education and Clinical Care
  • Solvay Pharmaceuticals
  • University of Washington
  • VA Puget Sound Health Care System

Registry information

Official study title

The Effect of Testosterone Treatment on Depressive Symptoms and Quality of Life in Older Men With Age-Related Hypogonadism and Subsyndromal Depression.

Important dates

Study start
2002
Primary completion
2005
Study completion
2006
First posted
Sep 20, 2005
Registry last updated
Oct 1, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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