Study to Improve Partner Services for STD Prevention
Status and phase
Conditions
Treatments
Study type
Funder types
Identifiers
Details and patient eligibility
About
The goal of this study was to examine the efficacy of patient-delivered partner treatment (PDPT) compared to standard partner referral (PR) and booklet enhanced partner referral (BEPR).
Full description
For partner treatment, index women who were diagnosed with trichomonas vaginalis and index men who were diagnosed with urethritis were randomized to one of three study arms:
Standard partner referral (PR) - index patients were instructed to tell their partners that they need to go to a clinic for STI evaluation and treatment.
Booklet-enhanced partner referral (BEPR) - index patients were given a wallet-sized booklet containing 4 tear-out cards with information for the partner and treatment guidelines for the providers that would see the partners. The partners could then present this card at a clinic to help the clinician better treat them. If index patients had more than 4 partners, they were given additional booklets.
Patient delivered partner treatment (PDPT) - index patients were given packages containing 2 gram metronidazole (for TV patients) or azithromycin 1 gram and cefixime 400 mg (for urethritis patients) for up to 4 identified sex partners. When cefixime was no longer available, ciprofloxacin 500 mg was used. These packages contained written instructions about how to take the medication, warnings about side effects and a nurse's pager number to call if there were any questions or if the partner encountered any problems. All medications were distributed in containers with childproof caps and the partner's initial and birthdates were written on the bottle. This was a requirement of the Louisiana State Pharmacy Board. Names were not documented on the index patient's study or medical records.
Sex
Ages
Volunteers
Inclusion criteria
- Woman attending Family Planning Clinic or men attending STD clinic
- Aged 16-44
- (non-pregnant women) - positive InPouch for trichomonas, or
- (pregnant women) - positive wet mount or InPouch for Trichomonas vaginalis
- (men) a complaint of urethritis which is verified on examination
- Report having >= 1sex partners in past 60 days
- Not presumptively treated for trichomonas (women) or urethritis (men)
- Provide informed consent to be re-contacted by telephone or in person in 14-28 days for a follow-up interview and T vaginalis or CT/GC rescreening
Exclusion criteria
Men
- Prisoner
- Has taken cefixime or azithromycin in last two weeks
- Has previously participated in the study
- All female partners are pregnant and did not have male partners Women
- client has taken metronidazole in the last two weeks
- client has been in this study previously
- women who are asymptomatic and in their first trimester of pregnancy
Trial design
Primary purpose
Allocation
Interventional model
Masking
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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