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Table 3 Association between baseline factors and failure to complete study

From: Participant characteristics associated with withdrawal from a large randomized trial of spermicide effectiveness

 

Total

Did not complete study

Relative Risk (95% confidence interval)

 

N

n

%

 

Age

    

   ≤25 years

660

317

48.0

1.29 (1.15 – 1.45)

   > 25 years

854

318

37.2

1

Relationship

    

   single not living with partner

522

247

47.3

1.21 (1.07 – 1.36)

   married or living with partner

992

388

39.1

1

Living children

    

   None

639

288

45.1

1.14 (1.0 1 – 1.28)

   Any

875

347

39.7

1

Baseline coital frequency

    

   ≥8 acts per month

862

389

45.1

1.21 (1.07 – 1.37)

   ≤7 acts per month

640

239

37.3

1

Geographic region of US

    

   West

424

215

50.7

1.28 (1.12 – 1.46)

   South

460

170

37.0

0.93 (0.80 – 1.09)

   Northeast

630

250

39.7

1

Center type

    

   university*

1069

476

44.5

1.25 (1.08 – 1.44)

   other

445

159

35.7

1

Recruitment rate at study site

    

   ≤4 per month

640

301

47.0

1.23 (1.09 – 1.38)

   > 4 per month

874

334

38.2

1

Reimbursement rate

    

   ≤$200

462

232

50.2

1.31 (1.16 – 1.47)

   >$200

1052

403

38.3

1

Participation in colposcopy study

    

   No

1381

590

42.7

1.26 (0.99, 1.61)†

   Yes

133

45

33.8

1

  1. *University centers were defined as those at which participants were seen in a primary university clinic setting. These included: University of Alabama at Birmingham, Birmingham, AL; University of Tennessee at Memphis, Memphis, TN; The University of Texas Health Science Center at San Antonio, San Antonio, TX; Baylor College of Medicine, Houston, TX; Medical University of South Carolina, Charleston, SC; University of Pittsburgh and the Magee-Womens Research Institute, Pittsburgh, PA; University of Pennsylvania Medical Center, Philadelphia, PA; University of Arizona Health Sciences Center, Tucson, AZ; NYU School of Medicine, New York, NY. Other centers included: Johns Hopkins Medical Services Corporation, Baltimore, MD; Vermont Women's Choice Program of Planned Parenthood, Burlington, VT; Eastern Virginia Medical School, Norfolk, VA; Minneapolis Medical Research Foundation, Minneapolis, MN; Planned Parenthood of Central and Northern Arizona, Phoenix, AZ
  2. †Although this confidence limit includes 1, the p-value for the association between this factor and early withdrawal was 0.047.