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HIV InfectionsPhase 2NCT00338767

Antidepressant Medication Plus Directly Observed Therapy for Improving Adherence to Antiretroviral Therapy

A Phase 2 study testing Directly Observed Therapy (DOT) and Fluoxetine in people with HIV Infections and Depression, run by Massachusetts General Hospital at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study will evaluate the effectiveness of directly observed therapy plus antidepressant medication in improving adherence to antiretroviral drug therapy among HIV-infected homeless and marginally housed people with depression. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
HIV Infections, Depression
What is being tested?
Directly Observed Therapy (DOT) and Fluoxetine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
150 participants
Where
1 siteUnited States
Study dates
Jan 2001to Aug 2006
Phase
Phase 2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Homeless or marginally housed
  • Score of greater than 13 on the Beck Depression Inventory (BDI)
  • DSM-IV diagnosis of major depressive disorder, dysthymia, or minor depressive disorder
  • Considered by the reviewing psychiatrist to benefit from antidepressant therapy
  • Willing to take antidepressant medication or, if currently taking medication, willing to change medications if deemed appropriate
  • Consents to coordinate with the primary medical provider
  • Speaks English

Who cannot join

  • Signs and symptoms consistent with diagnosis of dementia, as defined by DSM-IV
  • Current substance abuse disorder requiring immediate residential or inpatient treatment
  • At risk for suicide
  • Presence of signs and symptoms consistent with psychotic depression, as defined by DSM-IV, warranting immediate hospitalization
  • Any condition or use of any medication that may make simultaneous use of antidepressant medication unsafe
  • Currently prescribed antidepressant therapy and in psychiatric treatment (treated by a psychiatrist within 3 months prior to study entry)
Show all 9Show fewer
  • Pregnant
  • Bipolar disorder
  • Current psychotic disorder

Trial locations and contacts

1 site in 1 country.

United States1 site
  • UCSF Market Street Study Site

    San Francisco, California, 94102

Other trials in United States

About this study

Official title: Depression Treatment to Improve Antiretroviral Adherence

This study will evaluate the effectiveness of directly observed therapy plus antidepressant medication in improving adherence to antiretroviral drug therapy among HIV-infected homeless and marginally housed people with depression.

Read the detailed description

Antiretroviral drug therapy (ART) is a type of medication treatment for HIV that impairs the virus's ability to multiply. When used properly, it has been shown to be successful in reducing HIV-related deaths. A 95% adherence rate to ART is required to adequately suppress the virus and prevent transmission. Low ART adherence rates are often linked to depression, which is especially common in HIV-infected homeless or marginally housed people. In these cases, treatment with antidepressant medication may be useful in improving ART adherence. Directly Observed Therapy (DOT), in which medication intake is closely monitored, is another method of enhancing treatment compliance. DOT improved treatment adherence during the tuberculosis epidemic of the 1990s, and is now gaining recognition as a model for improving ART adherence. This study will evaluate the effectiveness of combining DOT and antidepressant medication in improving ART adherence among HIV-infected homeless and marginally housed people with depression.

Participants in this 9-month, open-label study will be randomly assigned to a treatment group or a control group. The control group will be given the phone number of the University of California, San Francisco AIDS Health Project (AHP) to call and make an appointment with a psychiatrist. Participants who attend appointments will be evaluated to determine their mental health status. Participants who are deemed to benefit from treatment will be scheduled for regular appointments at the AHP, but will be responsible for administering their own medications. The treatment group will meet with a study psychiatrist, who will prescribe an appropriate antidepressant medication. Subsequent meetings with the psychiatrist will occur weekly for the first 3 weeks, and then monthly for the duration of the study. Additionally, participants will have DOT visits every weekday morning for 1 month to take their antidepressant medications. After the first month, DOT visits will occur weekly or biweekly, depending on the medication regimen. If an individual does not attend a visit, study staff will try to locate the individual in the neighborhood to deliver the medication. Medication for the weekend will be prepared by study staff, but participants will take it on their own at home. For the last 2 months of the study, DOT visits will occur once monthly, at which time participants will receive their entire month's supply of medication.

Participants in both groups will be asked to report to the study site weekly for 6 months and then monthly for the final 3 months to provide an update on the status of their housing, healthcare providers, case managers, and HIV medications. Additional interviews about housing, income, use of health services, drug use, sexual practices, and mental health will occur at the beginning of the study and three more times throughout the study. Blood tests will be performed monthly to assess viral load, and every 3 months to assess CD4 count. Participants taking HIV medications will be visited by study staff at home once a month so that use of HIV medications can be determined. At the end of the study, participants in the control group may continue receiving treatment at the AHP. Six months after the end of the study, participants in the treatment group may also begin treatment with a psychiatrist at the AHP.

Being tested
Directly Observed Therapy (DOT), Fluoxetine
Keywords
AIDS, DOT, Directly Observed Therapy
Medical subject headings
HIV Infections, Depression, Acquired Immunodeficiency Syndrome, Directly Observed Therapy

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Directly Observed Therapy (DOT)Behavioural

    DOT includes storefront directly observed therapy of prescribed anti-depressants. Participants will meet with a study psychiatrist, who will prescribe an appropriate antidepressant medication. Subsequent meetings with the psychiatrist will occur weekly for the first 3 weeks, and then monthly for the duration of the study. Additionally, participants will have DOT visits every weekday morning for 1 month to take their antidepressant medications. After the first month, DOT visits will occur weekly or biweekly, depending on the medication regimen.

  • FluoxetineDrug

    Medication treatment includes flouxetine for treatment of depression.

Study groups in NCT00338767
Study groupRoleWhat they receive
TreatmentExperimentalParticipants receiving storefront directly observed therapy of anti-depressants (Fluoxetine)
Receives: Behavioral: Directly Observed Therapy (DOT); Drug: Fluoxetine
ControlNo interventionParticipants receiving referral to mental health follow-up with the UCSF AIDS Health Project

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Improved depression scores

    Measured: Measured at the end of 9 months

Secondary outcomes (2)
  1. HIV viral load

    Measured: Measured monthly for 9 months

  2. CD4 Count

    Measured: Measured at baseline and Months 3, 6, and 9

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Jun 2006 (estimated)
  2. Study startJan 2001
  3. Primary completionAug 2006
  4. Study completionAug 2006

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
150 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00338767
Sponsor's protocol ID
R01MH063011
Other IDs
R01MH063011
Status last verified
Nov 2013
First submitted
16 Jun 2006
Last updated
15 Nov 2013
Results posted
No
Data monitoring committee
No

Publications

  • Grelotti DJ, Hammer GP, Dilley JW, Karasic DH, Sorensen JL, Bangsberg DR, Tsai AC. Does substance use compromise depression treatment in persons with HIV? Findings from a randomized controlled trial. AIDS Care. 2017 Mar;29(3):273-279. doi: 10.1080/09540121.2016.1226479. Epub 2016 Sep 2.

    PubMed 27590273

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing Directly Observed Therapy (DOT) and Fluoxetine in people with HIV Infections and Depression, run by Massachusetts General Hospital at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 15 Nov 2013. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Improved depression scores (time frame: Measured at the end of 9 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00338767, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Nov 2013.

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