An interventional study of Physician self-disclosure of personal IUC use and Usual contraceptive counseling in Contraception, sponsored by University of Michigan. Completed at 1 site in United States. Open to female participants aged 18 Years to 44 Years. Per ClinicalTrials.gov, last updated 2013-11-25.
Sponsored by University of Michigan · Not applicable, Interventional, and Treatment
As many as one-third of female healthcare providers use intrauterine contraception (IUC), but only about 8 percent of US women overall do. This begs the question: Might physician self-disclosure of personal IUC use increase IUC use among patients? However, the positive or negative impact of physician self disclosure on IUC uptake or patient satisfaction is generally unknown. The purpose of this study was to evaluate if physician self-disclosure of personal IUC use increases patient use of IUC or impacts patients' satisfaction with their clinical encounter.
We performed a prospective randomized block design pilot trail of usual contraceptive counseling versus usual counseling plus physician self-disclosure of personal intrauterine contraceptive use.
University of Michigan is the lead sponsor of 1,475 studies on the registry; 196 are open to participants now.
Of its 162 completed or terminated interventional studies of FDA-regulated products, 128 (79%) have results posted.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
subjects received usual contraceptive counseling
Behavioral: Usual contraceptive counseling
subjects received usual contraceptive counseling plus intervention which was Physician self-disclosure of personal IUC use during the counseling
Behavioral: Physician self-disclosure of personal IUC use
Physicians self-disclosed personal intrauterine contraceptive use to subjects in intervention arm of study during contraceptive counseling
all subjects recieved usual contraceptive counseling
Also known as: contraceptive counseling
Intrauterine contraceptive use
All subjects were surveyed to determine use of intrauterine contraceptive immediately after their clinical visit where contraceptive counseling was received and at 2 months after their clinical encounter to assess intrauterine contraceptive use.
Time frame: immediately following clinical encounter and at 2 months
Satisfaction with clinical encounter
All subjects were surveyed to determine their with satisfaction with their overall clinical encounter immediately following their clinical encounter at at 2 months. Satisfaction was measured using a 5 point scale.
Time frame: immediately following clinical encounter and at 2 months
Satisfaction with contraceptive method
All subjects were surveyed to determine satisfaction with their contraceptive method of choice immediately following their clinical encounter and at 2 months. Satisfaction was measured using a 5 point scale.
Time frame: immediately following clinical enocunter and at 2 months
Satisfaction with provider
All subjects were surveyed to determine satisfaction with their provider immediately following their clinical encounter and at 2 months. Satisfaction was measured using a 5 point scale.
Time frame: immediately following clinical encounter and at 2 months
This study is completed, as verified in Nov 2013. You cannot join it, but the record below documents what was studied.
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University of Michigan