How to Trip Rapid Review

Step 1: Select articles relevant to your search (remember the system is only optimised for single intervention studies)

Step 2: press

Step 3: review the result, and maybe amend the or if you know better! If we're unsure of the overall sentiment of the trial we will display the conclusion under the article title. We then require you to tell us what the correct sentiment is.

1,469 results for

Postpartum Office Visit

by
...
Latest & greatest
Alerts

Export results

Use check boxes to select individual results below

SmartSearch available

Trip's SmartSearch engine has discovered connected searches & results. Click to show

21. Treatment of Depression During Pregnancy and the Postpartum Period

utilization including emergency department use, hospitalizations, and office visits • Adherence or persistence with treatment regimen Fetus, Infant, Child • Parameters at birth and up to 12 months of age: o Preterm birth (e.g., < 32 weeks, < 37 weeks) o Appropriate growth (height, weight, and head circumference) Source: http://effectivehealthcare.ahrq.gov Posted online: March 29, 2013 7 ? Gestational age (e.g., small for gestational age), race/ethnicity taken into consideration o Birth hospitalization (...) . Source: http://effectivehealthcare.ahrq.gov 13 Posted online: March 29, 2013 10. Ludermir AB, Lewis G, Valongueiro SA, et al. Violence against women by their intimate partner during pregnancy and postnatal depression: a prospective cohort study. Lancet. 2010 Sep 11;376(9744):903-10. PMID: 20822809. 11. Doucet S, Jones I, Letourneau N, et al. Interventions for the prevention and treatment of postpartum psychosis: a systematic review. Arch Womens Ment Health. 2011 Apr;14(2):89-98. PMID: 21128087. 12

2014 Effective Health Care Program (AHRQ)

22. Review of Evidence on Effective Postpartum Smoking Relapse Prevention Interventions

in smoking environment. 2 Executive Summary Research Question What are effective smoking relapse prevention interventions in pregnancy and the postpartum period up to twelve months? Context There are roughly 16,500 children born each year in Peel and in 2013 approximately 3% of pregnant women reported any smoking at their first prenatal visit, of which 31% reported at time of labour to having quit during pregnancy (1). However, lifestyle changes and stresses that arise in the postpartum period may lead (...) weeks postpartum among postpartum women who had quit smoking (intervention 81% vs. 46%, p Search Strategy: -------------------------------------------------------------------------------- 1 Smoking Cessation/ (20086) 2 exp Smoking/pc [Prevention & Control] (15214) 3 tobacco relapse.ab. (6) 4 smoking cessation.ab. (12747) 5 1 or 2 or 3 or 4 (34472) 6 exp Postpartum Period/ (48154) 7 Postnatal Care/ (3847) 8 exp Maternal Behavior/ (9918) 9 exp Parents/ (72341) 10 postnatal.ab. (68247) 11 postpartum.ab

2014 Peel Health Library

23. Home or Office Visit for the Insertion of Implantable Birth Control

post-implant insertion at the follow-up telephone call ] Assess rates of insertion of etonogestrel contraceptive implant in women randomly assigned to home visits or standard office visits. Secondary Outcome Measures : Interest in home visit option [ Time Frame: Within 6-8 weeks of enrollment ] Questionnaires will be distributed at enrollment (Enrollment Questionnaire) and at the insertion visit (Post-Implant Insertion Questionnaire) Rates of return for postpartum follow-up [ Time Frame: Within 6-8 (...) Home or Office Visit for the Insertion of Implantable Birth Control Home or Office Visit for the Insertion of Implantable Birth Control - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Home or Office Visit

2013 Clinical Trials

24. Postnatal depression screening in a paediatric primary care setting in Italy. Full Text available with Trip Pro

February and 31 July 2012, living in Italy's Milan-1 local health unit area, represented the target population of this pilot study. Parents attending well-child visits at any of the family paediatricians' offices between 60 to 90 days postpartum were asked to participate in the screening and to fill out the EPDS questionnaire. A cut-off score of 12 was used to identify parents with postnatal depression symptoms. Maternal and paternal socio-demographic variables and information concerning pregnancy (...) found to be positive for depressive symptoms. Women with mood disorders and anxiety during pregnancy were at increased risk of postpartum depression (OR 22.9, 95% CI 12.1-43.4). Only 11 mothers (8.7%) positive to EPDS screening attended a psychiatric service, and for 8 of them the diagnosis of postnatal depression was confirmed.The prevalence of postnatal depression was lower than previously reported. Routine screening resulted ineffective, since few mothers found positive for depression symptoms

2017 BMC Psychiatry

25. Safety of Minilaparotomy Provided by Trained Clinical Officers and Assistant Medical Officers: a Non-inferiority Trial

that tubal ligations by minilaparotomy (ML) conducted by trained clinical officers (COs) are no less safe as compared to those conducted by assistant medical officers (AMOs) in Tanzania. Participants will be randomized in a one to one ratio to ML by a CO and ML by an AMO. In addition to the screening and enrollment/ML visit, there will be three scheduled follow-up visits at 3, 7 and 42 days post-surgery. Condition or disease Intervention/treatment Phase Sterilization, Tubal Procedure: tubal ligation (...) in accordance with the Tanzania government guidelines; Able to understand study procedures and requirements of study participation; Agrees to return to the study site for the full schedule of follow-up visits after her ML procedure; Agrees to provide the study staff with an address, phone number, close relative, and/or other locator information while participating in the research study. Exclusion Criteria: Pregnancy Between 8 and 42 days postpartum or postabortion Known allergy or sensitivity to lidocaine

2016 Clinical Trials

26. Assessing the medium-term impact of a home-visiting programme on child maltreatment in England: protocol for a routine data linkage study. Full Text available with Trip Pro

Assessing the medium-term impact of a home-visiting programme on child maltreatment in England: protocol for a routine data linkage study. Child maltreatment involves acts of omission (neglect) or commission (abuse) often by caregivers that results in potential or actual harm to a child. The Building Blocks trial (ISRCTN23019866) assessed the short-term impact of an intensive programme of antenatal and postnatal visiting by specially trained nurses to support young pregnant women in England (...) . The Building Blocks: 2-6 Study will assess the medium-term impacts of the programme for mothers and children (n=1562), through the linkage of routinely collected data to the trial data, with a particular emphasis on the programme's impact on preventing child maltreatment.We have developed a bespoke model of data linkage whereby outcome data for the trial cohort will be retrieved by linked anonymous data abstraction from NHS Digital, Office for National Statistics and the Department for Education's National

2017 BMJ open

27. Improved postpartum care after a participatory facilitation intervention in Dar es Salaam, Tanzania: a mixed method evaluation Full Text available with Trip Pro

Improved postpartum care after a participatory facilitation intervention in Dar es Salaam, Tanzania: a mixed method evaluation In order to improve the health and survival of mothers/newborns, the quality and attendance rates of postpartum care (PPC) must be increased, particularly in low-resource settings.To describe outcomes of a collegial facilitation intervention to improve PPC in government-owned health institutions in a low-resource suburb in Dar es Salaam, Tanzania.A before-and-after (...) evaluation of an intervention and comparison group was conducted using mixed methods (focus group discussions, questionnaires, observations, interviews, and field-notes) at health institutions. Maternal and child health aiders, enrolled nurse midwives, registered nurse midwives, and medical and clinical officers participated. A collegial facilitation intervention was conducted and healthcare providers were organized in teams to improve PPC at their workplaces. Facilitators defined areas of improvement

2017 Global health action

28. Remote Surveillance of Postpartum Hypertension

will be scheduled for an office based nursing blood pressure visits 4-6 days postpartum. Care at this visit is based on a physician derived algorithm. Experimental: Remote (text based) surveillance Those randomized to remote surveillance will be provided with electronic blood pressure monitors prior to discharge and instructed on their use. Every day, for two weeks post-discharge, patients will receive a standard text message in the morning from a HIPAA compliant automated monitoring system reminding them (...) Summary: Women with hypertensive disorders of pregnancy need postpartum blood pressure (BP) surveillance to detect persistent hypertension. Various barriers result in only 30% attendance at postpartum BP visits. A more effective strategy is needed. Women with hypertension of pregnancy will be randomized to either text-based monitoring or office visits. Those randomized to the intervention will receive a BP cuff and text in their BP to an automated, clinician derived, HIPAA compliant text-based

2017 Clinical Trials

29. A randomized trial of single home nursing visits vs office-based care after nursery/maternity discharge: the Nurses for Infants Through Teaching and Assessment After the Nursery (NITTANY) Study. Full Text available with Trip Pro

A randomized trial of single home nursing visits vs office-based care after nursery/maternity discharge: the Nurses for Infants Through Teaching and Assessment After the Nursery (NITTANY) Study. To compare office-based care (OBC) with a care model using a home nursing visit (HNV) as the initial postdischarge encounter for "well" breastfeeding newborns and mothers.Randomized controlled trial.A single academic hospital.A total of 1154 postpartum mothers intending to breastfeed and their 1169 (...) newborns of at least 34 weeks' gestation.Home nursing visits were scheduled no later than 2 days after discharge; OBC timing was physician determined.Mothers completed telephone surveys at 2 weeks, 2 months, and 6 months. The primary outcome was unplanned health care utilization for mothers and newborns within 2 weeks of delivery. Other newborn outcomes were proportion seen within 2 days after discharge and breastfeeding duration. Maternal mental health, parenting competence, and satisfaction with care

2012 Archives of Pediatrics & Adolescent Medicine Controlled trial quality: predicted high

30. Postpartum Major Depression

. (From DSM-IV, p386) Concepts Mental or Behavioral Dysfunction ( T048 ) MSH ICD10 SnomedCT 268753005 , 154889000 , 192475007 , 147016002 , 191740008 , 58703003 English Postpartum Depression , Depression, Post-Natal , Depression, Post-Partum , Depression, Postnatal , Depression, Postpartum , Post Natal Depression , Post-Natal Depression , Post-Partum Depression , Postnatal Depression , Postnatal depression , Postnatal depressive disorder , DEPRESSION PUERPERAL , postpartum depression , postpartum (...) depression (diagnosis) , Depression puerperal , Depression, Postpartum [Disease/Finding] , depression postnatal , Depression;postnatal , Depression;puerperal , post partum depression , post-partum depression , postnatal blues , depression postpartum , post natal depression , post-natal depression , Post Partum Depression , Depression postpartum (excl psychosis) , [X]Postnatal depression NOS , [X]Postpartum depression NOS , Depression - postnatal , Postnatal depressive disorder (disorder) , Postnatal

2018 FP Notebook

31. Home or Office Etonogestrel Implant Insertion after Pregnancy: A Randomized Trial. (Abstract)

to detect a 40% difference in visit attendance, 20 women were assigned to each group. The secondary outcome was attendance of the 4-week postpartum visit.From June 2013 through February 2014, we screened 45 women and 40 were randomly assigned to home and office insertion visits. We enrolled 37 postpartum women and 3 women post-D&C. Because of the significant under enrollment of the latter, we chose to report results of only the postpartum women. The results were similar whether we included or excluded (...) post-abortion women. A majority of women desired a home visit for their implant insertion appointment at time of enrollment. Postpartum appointment attendance rates were similar between home and office visits at 53% and 50% (p=1.00), respectively. Home visits resulted in a trend toward increased implant uptake [12/19 (63%) vs 6/18 (33%), p=.10].Home insertion of the contraceptive implant may be a feasible option. Future studies that examine the feasibility and uptake in both postpartum and post-D&C

2016 Contraception Controlled trial quality: uncertain

32. Supporting Baby Behavior Through Pediatric Offices

postpartum ] Edinburgh Postnatal Depression Scale Maternal self-efficacy [ Time Frame: 1 week, 2 months, and 6 months postpartum ] Perceived Maternal Parenting Self-Efficacy Maternal perceived stress [ Time Frame: 1 week, 2 months, and 6 months postpartum ] Perceived Stress Scale Short-Form Infant sleep patterns [ Time Frame: 2 months and 6 months postpartum ] Brief Infant Sleep Questionnaire Infant development [ Time Frame: 2 months, 4 months, and 6 months postpartum ] Ages and Stages Questionnaire (...) Supporting Baby Behavior Through Pediatric Offices Supporting Baby Behavior Through Pediatric Offices - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Supporting Baby Behavior Through Pediatric Offices

2015 Clinical Trials

33. Influence of Ambient Temperature on Office Behaviors

intolerance? Do you have any religious affiliations that include specific food guidelines? Do you have any personal dietary restrictions, including but not limited to veganism? Have you participated in any weight-reduction program, weight-loss diet, or other special diet within the previous 3 months? Have you had weight loss or gain of >5% of body weight in the past 6 months for any reason except post-partum weight loss? Are you currently taking medication that suppresses or stimulates appetite (...) from the Nutrition Obesity Research Center? Are you currently pregnant or less than 3 months post-partum? Are you currently nursing or within 6 weeks of having completed nursing? Do you anticipate a pregnancy between time of screening and session date? Are you willing to report possible or confirmed pregnancies promptly at the time of the session? Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study

2015 Clinical Trials

34. Healthcare Utilization in the Postpartum Period Among Illinois Women with Medicaid Paid Claims for Delivery, 2009–2010 Full Text available with Trip Pro

delivering infants in Illinois in 2009-2010 were analyzed for the receipt, timing and patterns of postpartum care, as identified through International Classification of Diseases Revision 9-Clinical Modification and Current Procedural Terminology© codes for routine postpartum care (43.4 % of visits), other postpartum services (e.g., depression screening, family planning), and other office visits for non-acute care. Results Over 90,000 visits to 55,577 women were identified, with 81.1 % of women (...) experiencing any care during the first 90 days postpartum. Approximately 40 % had one visit, while 31 and 29 % had two and three or more visits, respectively. Thirty-four percent had their first visit <21 days postpartum, while 56 % had the first visit between 21 and 56 days postpartum. Compared with non-Hispanic whites, African-Americans had lower rates of receiving any care (73.6 vs. 86.5 %), fewer visits (48.0 vs. 33.5 % with only one visit), and later first visits (13.6 vs. 7.3 %, >56 days

2016 Maternal and child health journal

35. Postpartum Adherence Clubs to Enhance Support: the PACER Study

according to two finger-prick rapid tests using different test types (per routine protocol in this setting) or documentation of HIV status for those women self reporting HIV diagnosis. Initiated ART during the antenatal period (during most recent pregnancy) Within one month postpartum Currently breastfeeding within one month postpartum Willingness to return for postnatal study visits Able to provide informed consent for research Eligible to receive care at local Adherence Club, based on following local (...) the Standard of Care for Mothers. Details are provided in the intervention description. Infants receive the same care in each arm, according to the Standard of Care for Infants. Other: Standard of Care for Mothers Women will be referred immediately from the maternity ART clinic to their nearest adult ART clinic at their first postpartum clinic visit. At referral, they receive an initial 1-month supply of their current ART medication. At the first appointment after transfer into the general ART service

2015 Clinical Trials

36. Cost-Effectiveness of Immediate Compared With Delayed Postpartum Etonogestrel Implant Insertion. Full Text available with Trip Pro

were derived from a comprehensive literature review. We compared immediate (before discharge from the childbirth hospital stay) compared with delayed (at first postpartum office visit) postpartum placement of the contraceptive implant from a health care system's perspective. Implant insertion and removal, loss to follow-up at the postpartum visit, use of alternative contraceptive methods, and contraceptive failure were incorporated into the model. We calculated the incremental cost of immediate (...) Cost-Effectiveness of Immediate Compared With Delayed Postpartum Etonogestrel Implant Insertion. To evaluate the cost-effectiveness of immediate compared with delayed (6 weeks) postpartum etonogestrel implant insertion in preventing future unintended pregnancy.We constructed a decision-analytic model to examine a hypothetical population of women who request a contraceptive implant after giving birth. The timeframe for analysis was from the time of childbirth to 1 year postpartum. Model inputs

2015 Obstetrics and Gynecology

37. Follow up of Mothers Suspected of Postpartum Depression

after a positive PD screen. The objective of this study is to describe the rate at which mothers seek treatment for suspected PD after a positive screen at the pediatrician office. Additional examination will look at factors that predict whether a mother recalls a recommendation to seek treatment. Condition or disease Intervention/treatment Depression, Postpartum Other: telephone interview Detailed Description: The primary outcome of interest is whether mothers suspected of having PD seek treatment (...) Investigator: Nerissa S Bauer, MD, MPH Indiana University School of Medicine More Information Go to Layout table for additonal information Responsible Party: Nerissa Bauer, Assistant Professor, Indiana University ClinicalTrials.gov Identifier: Other Study ID Numbers: 1111007501 First Posted: September 25, 2015 Last Update Posted: September 25, 2015 Last Verified: September 2015 Additional relevant MeSH terms: Layout table for MeSH terms Depression Depressive Disorder Depression, Postpartum Behavioral

2015 Clinical Trials

38. Mother and Infant Home Visiting Program Evaluation-Strong Start

and Impact Findings from the Mother and Infant Home Visiting Program Evaluation-Strong Start. OPRE Report 2019-08. Washington, DC: Office of Planning, Research, and Evaluation, Administration for Children and Families, U.S. Department of Health and Human Services. Layout table for additonal information Responsible Party: Charles Michalopoulos, Chief Economist, MDRC ClinicalTrials.gov Identifier: Other Study ID Numbers: 2018.01.415.00 First Posted: March 3, 2014 Last Update Posted: February 6, 2019 Last (...) Visiting Program Evaluation-Strong Start The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02076204 Recruitment Status : Completed First Posted : March 3, 2014 Last Update Posted : February 6, 2019 Sponsor: MDRC Collaborators: Centers for Medicare and Medicaid Services Mathematica Policy Research, Inc

2014 Clinical Trials

39. Mother and Infant Home Visiting Program Evaluation

). The Mother and Infant Home Visiting Program Evaluation: Early Findings on the Maternal, Infant, and Early Childhood Home Visiting Program. OPRE Report 2015-11. Washington, DC: Office of Planning, Research and Evaluation, Administration for Children and Families, U.S. Department of Health and Human Services. Charles Michalopoulos, Kristen Faucetta, Carolyn J. Hill, Ximena A. Portilla, Lori Burrell, Helen Lee, Anne Duggan, and Virginia Knox. (2019). Impacts on Family Outcomes of Evidence-Based Early (...) Childhood Home Visiting: Results from the Mother and Infant Home Visiting Program Evaluation. OPRE Report 2019-07. Washington, DC: Office of Planning, Research, and Evaluation, Administration for Children and Families, U.S. Department of Health and Human Services. Other Publications: Charles Michalopoulos, Anne Duggan, Virginia Knox, Jill H. Filene, Helen Lee, Emily K. Snell, Sarah Crowne, Erika Lundquist, Phaedra S. Corso, Justin B. Ingels (2013). Revised Design for the Mother and Infant Home Visiting

2014 Clinical Trials

40. Harnessing the Power of Technology: MOMBA for Postpartum Smoking

management Traditional contingency management with financial incentives delivered in-person in the office for smoking cessation to postpartum women Behavioral: Office contingency management A control group which will receive financial incentives at an in-person office/clinic visit based on expired CO levels obtained through the Sensodrone™ CO sensor. Device: Sensordrone™ carbon-monoxide sensor Outcome Measures Go to Primary Outcome Measures : Acceptability [ Time Frame: 15 months ] Primary Outcome (...) of Technology: MOMBA for Postpartum Smoking The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02237898 Recruitment Status : Active, not recruiting First Posted : September 11, 2014 Last Update Posted : August 15, 2018 Sponsor: Yale University Collaborator: National Cancer Institute (NCI) Information provided

2014 Clinical Trials

To help you find the content you need quickly, you can filter your results via the categories on the right-hand side >>>>