scholarly journals Keywords to Recruit Spanish- and English-Speaking Participants: Evidence From an Online Postpartum Depression Randomized Controlled Trial

2014 ◽  
Vol 16 (1) ◽  
pp. e6 ◽  
Author(s):  
Alinne Z Barrera ◽  
Alex R Kelman ◽  
Ricardo F Muñoz
Keyword(s):  
Randomized Controlled Trial ◽  
Postpartum Depression ◽  
Controlled Trial ◽  
Randomized Controlled ◽  
English Speaking

scholarly journals Randomized controlled trial to prevent postpartum depression in adolescent mothers

2013 ◽  
Vol 208 (3) ◽  
pp. 192.e1-192.e6 ◽  
Author(s):  
Maureen G. Phipps ◽  
Christina A. Raker ◽  
Crystal F. Ware ◽  
Caron Zlotnick
Keyword(s):  
Randomized Controlled Trial ◽  
Postpartum Depression ◽  
Adolescent Mothers ◽  
Controlled Trial ◽  
Randomized Controlled

SECUREment bundles to prevent peripheral intravenous catheter failure—the SECURE-PIVC trial: study protocol for a pilot randomized controlled trial

2020 ◽  
Vol 29 (19) ◽  
pp. S40-S46
Author(s):  
Amanda Corley ◽  
Amanda J Ullman ◽  
Nicole Marsh ◽  
Larsen Emily N. ◽  
Gabor Mihala ◽  
...  
Keyword(s):  
Randomized Controlled Trial ◽  
Standard Care ◽  
Controlled Trial ◽  
Tertiary Hospital ◽  
Randomized Controlled ◽  
Rigorous Testing ◽  
Peripheral Intravenous Catheter ◽  
Catheter Failure ◽  
English Speaking ◽  
Pilot Randomized Controlled Trial

Introduction Peripheral intravenous catheters (PIVCs) are widely used, but failure is unacceptably common with up to 69% failing before treatment is complete. PIVC securement reduces failure, but the optimal way to achieve this is unclear. Tapes and supplementary securement products are widely used, however rigorous testing of these to reduce PIVC failure remains unexplored. Methods and analysis In adult medical-surgical wards at a tertiary hospital, this pilot randomized controlled trial tests standard care (bordered polyurethane dressing plus nonsterile tape over the extension tubing) against two securement interventions (intervention one: standard care plus two sterile tape strips over the PIVC hub; intervention two: intervention one plus a tubular bandage). Patients >18 years of age requiring a PIVC for >24 hours are eligible. Patients with laboratory-confirmed positive blood cultures within 24 hours of screening, known allergy to study products, current or high-risk of skin tear, or non-English speaking without interpreter are excluded. Sample size is 35 per trial arm, and central randomization is computer-generated with allocation concealed until entry. Patients and clinical staff cannot be blinded to treatment allocation. However, infection outcomes are assessed by a blinded investigator. Primary outcome is study feasibility. Secondary outcomes (PIVC failure, dwell time, skin adverse events, PIVC colonization, and cost) are compared between groups. Feasibility outcomes are reported descriptively. Ethics and trial commencement Ethical approvals were received from Royal Brisbane and Women's Hospital (HREC/18/QRBW/44571) and Griffith University (2018/1000). Trial commencement was May 2019. Trial registration: ACTRN12619000026123.

scholarly journals Randomized controlled trial to prevent postpartum depression in mothers on public assistance

2016 ◽  
Vol 189 ◽  
pp. 263-268 ◽  
Author(s):  
Caron Zlotnick ◽  
Golfo Tzilos ◽  
Ivan Miller ◽  
Ronald Seifer ◽  
Robert Stout
Keyword(s):  
Randomized Controlled Trial ◽  
Postpartum Depression ◽  
Public Assistance ◽  
Controlled Trial ◽  
Randomized Controlled

scholarly journals The effects of infant massage on maternal postpartum depression: A randomized controlled trial

2019 ◽  
Vol 8 (1) ◽  
pp. 28 ◽  
Author(s):  
FatemehSadat Hosseini-Baharanchi ◽  
ZibaRaisi Dehkordi ◽  
Afsaneh Kazemian ◽  
MohammadRahimi Madiseh ◽  
Marziye Reisi ◽  
...  
Keyword(s):  
Randomized Controlled Trial ◽  
Postpartum Depression ◽  
Controlled Trial ◽  
Infant Massage ◽  
Randomized Controlled ◽  
Maternal Postpartum Depression

scholarly journals Effectiveness of a Postpartum Text Message Program (Essential Coaching for Every Mother) on Maternal Psychosocial Outcomes: Protocol for a Randomized Controlled Trial (Preprint)

2021 ◽  
Author(s):  
Justine Dol ◽  
Megan Aston ◽  
Douglas McMillan ◽  
Gail Tomblin Murphy ◽  
Marsha Campbell-Yeo
Keyword(s):  
Social Support ◽  
Randomized Controlled Trial ◽  
Postpartum Depression ◽  
Self Efficacy ◽  
Controlled Trial ◽  
Text Message ◽  
Psychosocial Outcomes ◽  
Control Group ◽  
Depression And Anxiety ◽  
Randomized Controlled

BACKGROUND Women experience changes both physically and psychologically during their transition to motherhood. The postnatal period is a critical time for women to develop maternal self-efficacy. Mobile health interventions may offer a way to reach women during this critical period to offer support and information. Essential Coaching for Every Mother is a text message program that seeks to educate and support women during the first 6 weeks postpartum. OBJECTIVE The primary effectiveness objective is to compare the effectiveness of the Essential Coaching for Every Mother program on maternal psychosocial outcomes (self-efficacy, social support, postpartum depression, and postpartum anxiety) immediately after the intervention and 6 months postpartum, collectively as well as stratified by parity. The primary implementation objective is to evaluate the implementation extent and quality of the Essential Coaching for Every Mother program. METHODS This will be a hybrid type 1 effectiveness-implementation randomized controlled trial. A total of 140 mothers-to-be or new mothers from Nova Scotia will be recruited and randomized to the intervention or control arm, stratified by parity. The intervention arm will receive the Essential Coaching for Every Mother program, which consists of 53 messages sent twice a day for the first 2 weeks and daily for weeks 3 through 6. The control group will receive usual care. Messages are personalized based on the infant’s age and the woman’s self-selected preference for breastfeeding or formula feeding and tailored with the infant’s name and gender. Women can enroll in the program if they are ≥37 weeks pregnant or within 10 days postpartum, with the first message designed to be sent on the second evening after birth. The actual number of messages received will vary based on the timing of enrollment and the infant’s date of birth. Participants will complete questionnaires assessing self-efficacy, social support, and postpartum depression and anxiety at baseline (enrollment after birth) and 6 weeks (postintervention) and 6 months postpartum. Implementation data will be collected throughout the trial, and evaluation feedback will be collected at 6 weeks from women who received the intervention. RESULTS Recruitment for this study started on January 5, 2021, and is currently ongoing, with an anticipated date of recruitment completion of January 2022. CONCLUSIONS This study will assess the effectiveness of a postpartum text message program to improve maternal self-efficacy and social support while decreasing postpartum depression and anxiety. It will also shed light on the implementation effectiveness of the program. CLINICALTRIAL ClinicalTrials.gov NCT04730570; https://clinicaltrials.gov/ct2/show/NCT04730570 INTERNATIONAL REGISTERED REPORT DERR1-10.2196/27138

Internet‐based intervention for postpartum depression in China (“Mommy go”): Protocol for a randomized controlled trial

2020 ◽  
Vol 76 (9) ◽  
pp. 2416-2425
Author(s):  
Yu‐Hong Li ◽  
Ting‐Yu Mu ◽  
Liu Zhang ◽  
Cheng‐Lu Zhang ◽  
Dan Wu ◽  
...  
Keyword(s):  
Randomized Controlled Trial ◽  
Postpartum Depression ◽  
Controlled Trial ◽  
Randomized Controlled ◽  
Internet Based Intervention
Sign in / Sign up

Export Citation Format

Share Document