Trial Outcomes & Findings for Effect of Formal Contraception Handouts (NCT NCT03956030)
NCT ID: NCT03956030
Last Updated: 2023-03-30
Results Overview
Participants were sent a survey electronically at 8 weeks which asked the question "Now that you have delivered, are you currently using birth control? (yes or no)" The data table reflects the number who answered YES and the number who answered NO to this question per group.
TERMINATED
NA
8 participants
8 weeks postpartum
2023-03-30
Participant Flow
Participant milestones
| Measure |
Intervention
Intervention group will receive educational handout on contraception.
Contraception Handout: Handout covering contraception options
|
Control
Control group will receive educational handout on nutrition.
Nutritional Handout: Handout covering nutrition
|
|---|---|---|
|
Overall Study
STARTED
|
4
|
4
|
|
Overall Study
COMPLETED
|
1
|
1
|
|
Overall Study
NOT COMPLETED
|
3
|
3
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Effect of Formal Contraception Handouts
Baseline characteristics by cohort
| Measure |
Intervention
n=4 Participants
Intervention group will receive educational handout on contraception.
Contraception Handout: Handout covering contraception options
|
Control
n=4 Participants
Control group will receive educational handout on nutrition.
Nutritional Handout: Handout covering nutrition
|
Total
n=8 Participants
Total of all reporting groups
|
|---|---|---|---|
|
Age, Continuous
|
27.3 years
STANDARD_DEVIATION 6.9 • n=99 Participants
|
27.0 years
STANDARD_DEVIATION 5.1 • n=107 Participants
|
27.1 years
STANDARD_DEVIATION 5.6 • n=206 Participants
|
|
Sex: Female, Male
Female
|
4 Participants
n=99 Participants
|
4 Participants
n=107 Participants
|
8 Participants
n=206 Participants
|
|
Sex: Female, Male
Male
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
|
Ethnicity (NIH/OMB)
Hispanic or Latino
|
1 Participants
n=99 Participants
|
1 Participants
n=107 Participants
|
2 Participants
n=206 Participants
|
|
Ethnicity (NIH/OMB)
Not Hispanic or Latino
|
3 Participants
n=99 Participants
|
3 Participants
n=107 Participants
|
6 Participants
n=206 Participants
|
|
Ethnicity (NIH/OMB)
Unknown or Not Reported
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
|
Race (NIH/OMB)
American Indian or Alaska Native
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
|
Race (NIH/OMB)
Asian
|
1 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
1 Participants
n=206 Participants
|
|
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
|
Race (NIH/OMB)
Black or African American
|
1 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
1 Participants
n=206 Participants
|
|
Race (NIH/OMB)
White
|
1 Participants
n=99 Participants
|
4 Participants
n=107 Participants
|
5 Participants
n=206 Participants
|
|
Race (NIH/OMB)
More than one race
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
|
Race (NIH/OMB)
Unknown or Not Reported
|
1 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
1 Participants
n=206 Participants
|
PRIMARY outcome
Timeframe: 8 weeks postpartumPopulation: Subjects who completed the 8 week survey
Participants were sent a survey electronically at 8 weeks which asked the question "Now that you have delivered, are you currently using birth control? (yes or no)" The data table reflects the number who answered YES and the number who answered NO to this question per group.
Outcome measures
| Measure |
Intervention
n=1 Participants
Intervention group will receive educational handout on contraception.
Contraception Handout: Handout covering contraception options
|
Control
n=2 Participants
Control group will receive educational handout on nutrition.
Nutritional Handout: Handout covering nutrition
|
|---|---|---|
|
Contraception Use
Reported YES to contraception use
|
1 Participants
|
1 Participants
|
|
Contraception Use
Reported NO to contraception use
|
0 Participants
|
1 Participants
|
Adverse Events
Intervention
Control
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Dr. Christina DeAngelis
Penn State Health, Milton S. Hershey Medical Center
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place