Smartphone-based intervention for postpartum depressive symptoms (Smart-e-Moms): study protocol for a randomized controlled trial DOI Creative Commons

Daria Daehn,

Caroline Meyer,

Viola Loew

et al.

Trials, Journal Year: 2024, Volume and Issue: 25(1)

Published: July 10, 2024

Abstract Background Postpartum depression constitutes a significant public health issue, with prevalence rates ranging between 8 and 19% in high-income nations. Nevertheless, numerous barriers, including time constraints, societal stigmatization, feelings of shame, contribute to the limited utilization healthcare services during postpartum period. Digital interventions offer an opportunity enhance care for women experiencing depressive symptoms. Methods We will conduct two-arm randomized controlled trial assess effectiveness smartphone-based intervention comparison treatment-as-usual control group Germany. Our aim is randomize 556 participants 1:1 ratio. Participants be provided access preventive called “Smart-e-Moms,” which incorporates therapeutic support comprises 10 concise modules rooted cognitive-behavioral therapy. For group, evaluations take place at baseline (t0), prior sessions 4 (intermediate assessments), upon completing 6 weeks after (t1). The group’s assessments (t0) baseline. Follow-up are scheduled 12 24 from examine short-term stability any observed effects. anticipate that exhibit improvements their symptoms (as measured Edinburgh Postnatal Depression Scale). Additionally, we analyze secondary outcomes, maternal bonding, stress levels, self-efficacy, satisfaction intervention, utilization. Discussion If Smart-e-Moms proves effective, it has potential play role within German-speaking regions. Ideally, this could not only benefit well-being but also improve prospects healthy child development. Trial registration German clinical trials registry DRKS00032324. Registered on January 26, 2024.

Language: Английский

Smartphone-based intervention for postpartum depressive symptoms (Smart-e-Moms): study protocol for a randomized controlled trial DOI Creative Commons

Daria Daehn,

Caroline Meyer,

Viola Loew

et al.

Trials, Journal Year: 2024, Volume and Issue: 25(1)

Published: July 10, 2024

Abstract Background Postpartum depression constitutes a significant public health issue, with prevalence rates ranging between 8 and 19% in high-income nations. Nevertheless, numerous barriers, including time constraints, societal stigmatization, feelings of shame, contribute to the limited utilization healthcare services during postpartum period. Digital interventions offer an opportunity enhance care for women experiencing depressive symptoms. Methods We will conduct two-arm randomized controlled trial assess effectiveness smartphone-based intervention comparison treatment-as-usual control group Germany. Our aim is randomize 556 participants 1:1 ratio. Participants be provided access preventive called “Smart-e-Moms,” which incorporates therapeutic support comprises 10 concise modules rooted cognitive-behavioral therapy. For group, evaluations take place at baseline (t0), prior sessions 4 (intermediate assessments), upon completing 6 weeks after (t1). The group’s assessments (t0) baseline. Follow-up are scheduled 12 24 from examine short-term stability any observed effects. anticipate that exhibit improvements their symptoms (as measured Edinburgh Postnatal Depression Scale). Additionally, we analyze secondary outcomes, maternal bonding, stress levels, self-efficacy, satisfaction intervention, utilization. Discussion If Smart-e-Moms proves effective, it has potential play role within German-speaking regions. Ideally, this could not only benefit well-being but also improve prospects healthy child development. Trial registration German clinical trials registry DRKS00032324. Registered on January 26, 2024.

Language: Английский

Citations

0