- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00677742
The Impact of Pack Supply on Birth Control Pill Continuation (SixPack)
Impact of Pack Supply on Oral Contraception Continuation
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Discontinuation of oral contraceptive use in the initial months is common; successful early continuation is predictive of long term continuation and prevention of unintended pregnancy. The conventional approach to initiation of hormonal contraceptives in publicly funded clinics across the United States is to give the patient a limited supply of OCs, or a prescription with a limited number of refills, and then have her return to the clinic for a refill. This approach requires the patient to make frequent visits to the clinic, a barrier to method continuation.
This randomized trial will evaluate a simple but potentially powerful change in family planning clinic practice, i.e., the effect of dispensing more versus fewer cycles of oral contraception (OC). The study will be carried out in an urban, publicly funded family planning clinic that serves a population that is poor, young and primarily Hispanic or AfricanAmerican. This population was targeted as its members are at increased risk of discontinuing contraception in the first year of use.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
-
-
New York
-
New York, New York, Forenede Stater, 10032
- Columbia University Medical Center, Family Planning Clinic
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- English or Spanish speaker
- age less than or equal to 35 years requesting OC as their primary method of contraception
- currently sexually active or anticipating sexual activity within the next 30 days
Exclusion Criteria:
- contraindications to oral contraceptives per clinic protocol (e.g., hypertension and pregnancy)
- currently using OCs (that is, current users requesting a routine refill)
- desiring pregnancy within the next 6 months
- leaving the clinic catchment area within 6 months
- previous participation in this study
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: 1
enhanced initial supply of oral contraception
|
7 packs of pills, or 1 pack of pills and a prescription for 6 refills
|
|
Aktiv komparator: 2
conventional initial supply of oral contraception
|
3 packs of pills, or 1 pack of pills and a prescription for 2 refills
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
oral contraception continuation
Tidsramme: 6 months
|
6 months
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Katharine O'Connell, MD, MPH, Columbia University
Publikationer og nyttige links
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- AAAC1723
- 1 FPRPA0060250100
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