Clinical trials: Contraceptive Behavior
Pregnancy Prevention, Sexual Behavior
Project Legacy Impact Evaluation Study
This study will design and rigorously evaluate the efficacy of Project Legacy, a five week positive youth development intervention to decrease sexual risk for unintended pregnancies and STIs among youth experiencing homelessness…
- Conditions
- Pregnancy Prevention, Sexual Behavior, Contraception Behavior, Sexually Transmitted Diseases
- Trial name
- NCT03366636
- Testing
- Project Legacy
- Where
- 12 sites in United States
- Volunteers
- 571 people, healthy volunteers welcome
- Sponsor
- Children's Hospital Los Angeles
Contraception
Continuous Versus Cyclic Use of Oral Contraceptive Pills in Adolescents
The primary purpose of this study is to compare the compliance rates of adolescents who take oral contraceptives (OCPs) continuously to those who take OCPs cyclically.
- Trial name
- NCT00326404
- Testing
- Desogestrel-Ethinyl Estradiol 21 tablets, Desogestrel-Ethinyl Estradiol 28 tablets
- Where
- Canada
- Volunteers
- 130 people
- Sponsor
- The Hospital for Sick Children
Contraception Behavior
Utility of Immediate Post Placental Insertion of Intrauterine Device During Cesarean Delivery
Iraq is a country that ranks 33rd around world population growth rate. Meanwhile it is one of the counties in the middle east with the highest fertility rate, In addition to the considerable number of unintended pregnancy mainly…
- Trial name
- NCT04136613
- Testing
- Copper Intra uterine contarceptive device ( Cu-T 380A)
- Where
- Iraq
- Volunteers
- 150 people
- Sponsor
- Taghreed Alhaidari
Anti-Infective Agents, Anti-Retroviral Agents
Safety, PK, and PD Study of IVRs Releasing TFV and LNG
This multi-center Phase I study is designed to characterize the safety, PK, and PD of TFV/LNG IVR to assess systemic and genital tract bioavailability in healthy women.
- Conditions
- Anti-Infective Agents, Anti-Retroviral Agents, Contraceptive Usage
- Trial name
- TFV/LNG IVR (NCT03279120)
- Testing
- TFV/LNG IVR
- Where
- 2 sites in United States, Dominican Republic
- Volunteers
- 66 people, healthy volunteers welcome
- Sponsor
- CONRAD
Contraception, Contraception Behavior
The Over The Counter Pill National Study
This is a prospective cohort study of individuals purchasing the oral contraceptive pill over the counter (OTC) in pharmacies in 32 US states. The comparison group is people receiving a prescription (Rx) for oral contraception.
- Conditions
- Contraception, Contraception Behavior, Contraceptive Usage, Health Care Utilization
- Trial name
- NCT05988983
- Testing
- Availability of OTC contraceptive pill
- Where
- United States
- Volunteers
- 1,026 people, healthy volunteers welcome
- Sponsor
- Oregon Health and Science University
Contraceptive Usage, Contraception
SexHealth Mobile: Integrating a Mobile Clinic and a Point-of-care Contraception Counseling and Access
Pilot study aims to evaluate the effectiveness of "SexHealth Mobile" and improve access to highly effective contraception among women with substance use disorder (SUD) with "SexHealth Mobile" intervention.
- Trial name
- NCT04227145
- Testing
- SexHealth Mobile
- Where
- 4 sites in United States
- Volunteers
- 98 people
- Sponsor
- Children's Mercy Hospital Kansas City
Contraceptive Usage
Essure Transvaginal Ultrasound (TVU) Study
The Essure procedure, FDA approved since 2002 and CE Mark approved since 2001, is the first permanent birth control method that can be performed in the comfort of a physician's office without hormones, cutting, burning or the…
- Trial name
- NCT01327105
- Testing
- TVU
- Where
- 21 sites in United States, Canada and 2 more
- Volunteers
- 547 people, healthy volunteers welcome
- Sponsor
- Bayer
Contraceptive Usage
Immediate Versus Delayed Insertion of Intrauterine Contraception After Medical Abortion
PICO: Population: Women with unwanted pregnancy having a medical abortion and fulfilling inclusion and without exclusion criteria and opting for IUC as post abortion contraception.
- Trial name
- INTRAM (NCT03603145)
- Testing
- Immediate insertion
- Where
- 6 sites in Sweden
- Volunteers
- 720 people
- Sponsor
- Karolinska Institutet
Contraception Behavior
An mHealth Trial to Promote the Use of Postpartum Contraception
Multiple encounters of pregnant women with the health care system during the late antenatal and immediate postpartum period provide a gateway for postpartum family planning counselling.
- Trial name
- PPFP (NCT03612518)
- Testing
- Text and Voice Messages, Interactive Phone Call
- Where
- 4 sites in Pakistan
- Volunteers
- 970 people
- Sponsor
- Junaid-ur-Rehman Siddiqui
Contraception, Contraception Behavior
Contraception for Solid Organ Transplant Patients: Utilizing Social Media
The purpose of this study is to use an electronic survey to explore Solid Organ Transplant patients' contraceptive knowledge and counseling.
- Conditions
- Contraception, Contraception Behavior, Contraceptive Usage, Reproductive Health
- Trial name
- NCT03979950
- Testing
- Survey
- Where
- United States
- Volunteers
- 52 people, healthy volunteers welcome
- Sponsor
- University of California, San Diego
Oral Contraception
The Impact of Pack Supply on Birth Control Pill Continuation
The purpose of this study is to determine whether getting more packs of birth control pills leads to improved continuation, when compared with getting the traditional supply.
- Trial name
- SixPack (NCT00677742)
- Testing
- enhanced initial supply of oral contraception, conventional initial supply of oral contraception
- Where
- United States
- Volunteers
- 700 people
- Sponsor
- Columbia University
Contraceptive Usage, Family Planning
Effect of Male Involvement in Family Planning Education on Contraceptive Use
This study aimed to examine the effect of Male Involvement in Family Planning Education on Contraceptive Use Among Married Couples in the Pastoralist Community of Fentale District, Eastern Ethiopia.
- Trial name
- NCT06450756
- Testing
- Couples arm, Male arm
- Where
- Ethiopia
- Volunteers
- 1,496 people
- Sponsor
- Jimma University
Emergency Contraception
A Study of Use of Ella®, an Emergency Contraceptive, Under Simulated OTC Conditions
This study is designed to assess whether consumers select and use ella® (ulipristal acetate 30mg), an emergency contraceptive, in a manner consistent with the OTC package directions in an OTC-like setting.
- Trial name
- LIBRella (NCT03208985)
- Testing
- Use Phase (Ulipristal Acetate, 30 mg)
- Where
- 34 sites in United States
- Volunteers
- 1,270 people, healthy volunteers welcome
- Sponsor
- HRA Pharma
Contraceptive Usage, Overweight or Obesity
A 6-month Observational Study on Combined Oral Contraceptives and Body Weight in Pre-Menopausal Women With Overweight or Obesity
Approximately 15 million women of reproductive age women in the United States have overweight or obesity and use the combined estrogen and progestin oral contraceptive pill (COC).
- Conditions
- Contraceptive Usage, Overweight or Obesity, Body Weight Changes, Appetitive Behavior
- Trial name
- NCT05061472
- Where
- 2 sites in United States
- Volunteers
- 20 people
- Sponsor
- University of Colorado, Denver
Contraceptive Usage
Disparities in Emergency Contraceptive Metabolism Dictate Efficacy
The purpose of this study is to learn more about why some people are at greater risk for oral emergency contraceptive failure while others are not.
- Trial name
- NCT05674513
- Testing
- Ulipristal acetate
- Where
- United States
- Volunteers
- 140 people, healthy volunteers welcome
- Sponsor
- Oregon Health and Science University
Pre-Exposure Prophylaxis, STI
Community-based Venues for Delivery of Healthcare Services: Proof of Concept Pilot
The investigators propose to offer a package of evidence-based health services to women in two hair salons in the Umlazi township of Durban.
- Conditions
- Pre-Exposure Prophylaxis, STI, Contraceptive Usage
- Trial name
- NCT04222504
- Testing
- Provision of sexual health preventative services in the salon setting
- Where
- South Africa
- Volunteers
- 436 people, healthy volunteers welcome
- Sponsor
- Massachusetts General Hospital
Complications; Contraceptive, Female Lactation
Early Versus Standard Postpartum Insertion of the Etonogestrel Contraceptive Implant
A highly effective single rod contraceptive implant is now available for use in the US. Delays in the insertion of the device until later in the postpartum period may negatively impact initiation rates.
- Trial name
- NCT00847587
- Testing
- Etonogestrel contraceptive implant
- Where
- United States
- Volunteers
- 69 people, healthy volunteers welcome
- Sponsor
- University of Utah
Female Contraception
Oral Contraceptives and Economic Behaviour
The investigators aim is to evaluate effects of combined oral contraceptives (OC) on mood, sexuality and economic behaviour in a randomized, double-blind, placebo-controlled study.
- Trial name
- P-piller101 (NCT02257671)
- Testing
- Oral contraceptive
- Where
- Sweden
- Volunteers
- 400 people, healthy volunteers welcome
- Sponsor
- Karolinska University Hospital
Depression, Postpartum, Anxiety, Postpartum
Efficacy of Mother's Time in Ethiopia
Mother's Time is an evidence-based cognitive behavioral therapy (CBT) tool designed to support postpartum women experiencing mild to moderate symptoms of stress, depression or anxiety.
- Conditions
- Depression, Postpartum, Anxiety, Postpartum, Contraceptive Usage
- Trial name
- NCT05806463
- Testing
- Mother's Time
- Where
- Ethiopia
- Volunteers
- 328 people
- Sponsor
- Johns Hopkins Bloomberg School of Public Health
Premenstrual Syndrome, Depression
The Oral Contraceptive Pill for Premenstrual Worsening of Depression
To determine if augmentation with the oral-contraceptive pill containing drospirenone and ethinyl estradiol is more effective than placebo in the treatment of premenstrual breakthrough of depression.
- Trial name
- NCT00633360
- Testing
- Drospirenone and ethinyl estradiol
- Where
- United States
- Volunteers
- 32 people
- Sponsor
- Massachusetts General Hospital