26 research outputs found
A Randomized Controlled Trial to Compare Computer-assisted Motivational Intervention with Didactic Educational Counseling to Reduce Unprotected Sex in Female Adolescents
Study Objective: To examine a computer-assisted, counselor-guided motivational intervention (CAMI) aimed at reducing the risk of unprotected sexual intercourse.
Design, Setting, Participants, Interventions, and Main Outcome Measures: We conducted a 9-month, longitudinal randomized controlled trial with a multisite recruitment strategy including clinic, university, and social referrals, and compared the CAMI with didactic educational counseling in 572 female adolescents with a mean age of 17 years (SD = 2.2 years; range = 13-21 years; 59% African American) who were at risk for pregnancy and sexually transmitted diseases. The primary outcome was the acceptability of the CAMI according to self-reported rating scales. The secondary outcome was the reduction of pregnancy and sexually transmitted disease risk using a 9-month, self-report timeline follow-back calendar of unprotected sex.
Results: We conducted a 9-month, longitudinal randomized controlled trial with a multisite recruitment strategy including clinic, university, and social referrals, and compared the CAMI with didactic educational counseling in 572 female adolescents with a mean age of 17 years (SD = 2.2 years; range = 13-21 years; 59% African American) who were at risk for pregnancy and sexually transmitted diseases. The primary outcome was the acceptability of the CAMI according to self-reported rating scales. The secondary outcome was the reduction of pregnancy and sexually transmitted disease risk using a 9-month, self-report timeline follow-back calendar of unprotected sex.
Conclusion: Among those who completed the intervention, the CAMI reduced unprotected sex among an at-risk, predominantly minority sample of female adolescents. Modification of the CAMI to address methodological issues that contributed to a high drop-out rate are needed to make the intervention more acceptable and feasible for use among sexually active predominantly minority, at-risk, female adolescents
A Double‐Blind Randomized Placebo‐Controlled Trial of Oral Naltrexone for Heavy‐Drinking Smokers Seeking Smoking Cessation Treatment
Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/137315/1/acer13396.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/137315/2/acer13396_am.pd
Quit intention as a predictor of quit attempts over time in adolescents with psychiatric disorders.
Affective salience of outcome expectancies for smoking:An implicit measure of motivation to change
Affective salience of outcome expectancies for smoking:An implicit measure of motivation to change
Quit intention as a predictor of quit attempts over time in adolescents with psychiatric disorders.
BACKGROUND: Rates of smoking among adolescents with psychiatric comorbidity are high, despite the well-known health risks. The current longitudinal study examined patterns of quitting behavior in adolescent smokers with psychiatric comorbidity. METHODS: The study evaluated 191 inpatient adolescents who had been enrolled in a randomized controlled trial of motivational interviewing versus brief advice for smoking cessation, and assessed their intentions to quit smoking. RESULTS: Rates of quit attempts at post-hospital, 1-month, and 6-month assessments were 23%, 17%, and 17%, respectively. Adolescents who reported an intention to quit smoking (43%) were significantly more likely to report a quit attempt, regardless of psychiatric symptoms, cognitive factors, or substance use. CONCLUSIONS: Intention to quit smoking appears to translate to substantial quit behavior, even in a high-risk adolescent population that may otherwise be viewed as uninterested in quitting, suggesting the need to proactively connect this population with adequate services and follow-up support. (Am J Addict 2013;XX:1-6)
General and religious coping predict drinking outcomes for alcohol dependent adults in treatment
LoTTS parent-infant interaction coding scale: Ease of use and reliability in a sample of high-risk mothers and their infants
Reliable and valid measurement of parent-infant interactions is necessary to demonstrate parental skill acquisition, but existing observational coding schemes are too complex for practical use in most human service settings. The LoTTS Parent-Infant Interaction Coding System (LPICS) was developed specifically to require minimal training and to be maximally useful for human service (rather than research) settings. The LPICS consists of three global scales and four behavioral counts. Undergraduate students participated in approximately 9Â h of training and coding using the LPICS. Low inter-rater reliability scores initially necessitated modifications to the LPICS in order to enhance reliability. The revised scoring procedure showed more promise, particularly for three behavior counts: talking to the infant (ICCÂ =Â .86, excellent), touching the infant (ICCÂ =Â .90, excellent), and smiling at the infant (ICCÂ =Â .66, good), and one global scale: parental warmth (ICCÂ =Â .58, fair). The revised LPICS may have utility as a brief, simple, and easy-to-teach observational measure of parent-infant interactions.Parent-infant interaction Coding systems Inter-rater reliability Ease of use