Clinical Trials Logo

Clinical Trial Summary

Low income mothers of young children represent a disadvantaged group who are at exceptional risk for depressive syndromes and who have increasingly limited access to mental health services. The proposed project is designed to evaluate Mom-Net, an internet-facilitated cognitive-behavioral(CBT) intervention for depression, adapted from Lewinsohn's Coping with Depression Course, and tailored to mothers of young children. Mom-Net, which was developed and piloted in an recently completed NIMH-funded investigation (MH070426), was designed to overcome the substantial barriers to treatment participation that exist for mothers experiencing economic hardship and those in rural communities. Though the pilot trial demonstrated that the program was very effective in reducing depressive symptoms and related difficulties, it was conducted under the 'idealized' conditions typical of initial intervention tests (e.g., computers and internet connections were supplied to all participants; access to the internet was provided by a single browser; coaches who provided weekly phone support were research staff, and initial recruitment and motivational interviews sessions were conducted via home visits to participants). These conditions likely facilitated recruitment and retention of participants, as well as ease and fidelity of treatment delivery. Thus one goal of the current project is to evaluate the intervention under conditions that are closer to those of real-world service providers and recipients. The current project is also intended to provide a more rigorous test of the intervention than did the pilot in a number of ways. Participants in the pilot trial will be 300 mothers of 3-5 year old children recruited through Head Start classrooms and prescreened for the presence of elevated depressive symptoms.Subsequent to the pre-intervention assessment, participants will be randomized to either the intervention or facilitated usual care (FUC) condition. The evaluation of the intervention will focus on maternal depressive symptoms, parenting behavior, and child adjustment. Two follow-up assessments (at 12-month and 24-month intervals) will enable us to examine maintenance of effects. Overall, the investigation will contribute to the evidentiary base regarding the dissemination potential of this empirically-supported intervention, adaptations to which have the potential to enable a greater proportion of the population to access and benefit from it.


Clinical Trial Description

The project is designed to evaluate Mom-Net, an internet-facilitated cognitive-behavioral (CBT) intervention for depression, adapted from Lewinsohn's Coping with Depression Course, and tailored to mothers of young children. Mom-Net, which was developed and piloted in a recently completed NIMH-funded investigation (MH070426), was designed to overcome the substantial barriers to treatment participation that exist for mothers experiencing economic hardship and those in rural communities. Though the pilot trial demonstrated that the program was very effective in reducing depressive symptoms and related difficulties, it was conducted under the 'idealized' conditions typical of initial intervention tests (e.g., computers and internet connections were supplied to all participants; access to the internet was provided by a single browser; coaches who provided weekly phone support were research staff, and initial recruitment and motivational interviews sessions were conducted via home visits to participants). These conditions likely facilitated recruitment and retention of participants, as well as ease and fidelity of treatment delivery. Thus one goal of the current project is to evaluate the intervention under conditions that are closer to those of real-world service providers and recipients. The current project is also intended to provide a more rigorous test of the intervention than did the pilot in a number of ways. Participants in this project will be 300 mothers of 3-5 year old children recruited through Head Start classrooms and prescreened for the presence of elevated depressive symptoms. Subsequent to the pre-intervention assessment, participants will be randomized to either the intervention or facilitated usual care (FUC) condition. The evaluation of the intervention will focus on maternal depressive symptoms, parenting behavior, and child adjustment. Two follow-up assessments (at 12-month and 24-month intervals) will enable us to examine maintenance of effects. Overall, the investigation will contribute to the evidentiary base regarding the dissemination potential of this empirically-supported intervention, adaptations to which have the potential to enable a greater proportion of the population to access and benefit from it. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01535352
Study type Interventional
Source Oregon Research Institute
Contact
Status Completed
Phase N/A
Start date September 2012
Completion date April 2017

See also
  Status Clinical Trial Phase
Not yet recruiting NCT05490056 - Adequacy of Antenatal Care and Its Determinants in Assiut District
Completed NCT02938598 - Motivating Our Mothers 2 N/A
Recruiting NCT05565196 - Birth Companion Intervention in Ethiopia, Kenya and Nigeria N/A
Completed NCT03389958 - Maternity Care and Contraception N/A
Not yet recruiting NCT06054412 - An Adjunctive Neurofeedback Training Program to Enhance Wellness Among Trauma-Exposed Postpartum Mothers N/A
Completed NCT02501252 - Effectiveness and Acceptability of Availing Skilled Birth Attendance (SBA) Services Through Community Reproductive Health Nurses (CORN) to a Household Level at Rural Communities of Ethiopia; A Cluster Community Trial in Gedeo Zone, SNNPR N/A
Active, not recruiting NCT04421235 - Expanding Knowledge About and Evaluating Services for Incarcerated Pregnant and Postpartum Women in Arkansas N/A
Completed NCT04576364 - 12-hour Versus 24-hour Postpartum Magnesium Sulphate for Preeclamptic Patients N/A
Recruiting NCT06035315 - The 1000 First Day of Life : Effect of Multi Micronutrients Supplementation on Pregnancy Outcomes N/A
Recruiting NCT05484726 - Maternal Role in Oral Feed Establishment in Preterm Neonates N/A
Recruiting NCT05365815 - Melanated Group Midwifery Care (MGMC) N/A
Active, not recruiting NCT05782660 - Cash Benefits and Reproductive/Perinatal Health N/A
Recruiting NCT05206552 - The Correlation Between Maternal Infant Bonding, Pain and Postpartum Depression
Completed NCT06217653 - Baby Yoga Sleep Maternal Attachment Breastfeeding N/A
Recruiting NCT05474534 - An Intervention to Enhance Well-Being in Trauma Exposed New Mothers N/A
Active, not recruiting NCT04601987 - Healthy Moms: Prenatal Counseling for Postpartum Health N/A
Active, not recruiting NCT03890653 - Impact Evaluation of the Nigeria Result-Based Financing Project N/A