Washington Hospital Center
Washington D.C., District of Columbia, 20010, United States
NCT Number: NCT05503056
This is a prospective study examining the potential impact art therapy has on postpartum depression and mother-baby bonding in women. Women who receive care at Washington Hospital Center's will be recruited for this study.
Looking for future studies?
Notify Me18 year and older
Female
Interventional
Not applicable
Washington D.C., District of Columbia, 20010, United States
The purpose of this research study is to assess whether alternative mental health interventions positively impacts maternal-infant bonding and postpartum depression rates in women. Postpartum depression continues to be a prevalent concern for mothers and families in the United States, with current estimates demonstrating 10-20% of women being diagnosed within one year of birth. The risks of developing postpartum depression are not well known, with maternal anxiety and stress during pregnancy being one of the proposed predisposing factors. Women with high-risk pregnancies are particularly susceptible to higher levels of stress and depression, during their pregnancy thus leaving them at great risk for postnatal depression. Given this association, finding ways to alleviate stressors is important.
Music therapy is a known intervention linked with improved outcomes in women undergoing procedural interventions, including labor and delivery. Art therapy is also associated with improved outcomes, though outside of obstetrics. In elderly women with depression and those with breast cancer diagnoses, visual art therapy has been shown to be superior to other non-medicinal interventions in improving mood. Current data is both qualitative as well as quantitative, demonstrating positive impacts on patients.
While evidence exists to support the utilization of these alternative forms of therapy, they have not been adequately applied to pregnant and postpartum women outside of music therapy. With the understanding that other art forms are tied with improvement in anxiety, depression, and quality of life, the implementation in this special patient population is paramount. Investigating how a relatively benign intervention can possibly promote improvement in maternal mental health, thus allowing for better mother-baby bonding in the first year of life, is key in finding ways to support the growth and development of healthy families.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
six sessions of art therapy with licensed therapists
no intervention to this group
Time frame: start, and end of intervention period; time of delivery, two weeks postpartum, six weeks postpartum, three months postpartum
raw score on scale
Time frame: start, and end of intervention period; time of delivery, two weeks postpartum, six weeks postpartum, three months postpartum
raw score on scale
Time frame: start, and end of intervention period; time of delivery, two weeks postpartum, six weeks postpartum, three months postpartum
chart review to see if patients utilized services "yes" vs. "no"
Time frame: start, and end of intervention period; time of delivery, two weeks postpartum, six weeks postpartum, three months postpartum
chart review to see if patients utilized services "yes" vs. "no"
Time frame: up to 3 months postpartum
chart review
Time frame: delivery
chart review
Time frame: delivery
chart review
Time frame: delivery
chart review
Time frame: delivery
chart review
Time frame: delivery
chart review
Time frame: delivery
chart review
Time frame: delivery
chart review
Medstar Health Research Institute
Other
The Utilization of Art Therapy During Pregnancy to Reduce the Incidence of Postpartum Depression
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT04364646
Behavior, Behavioral Symptoms
Glen Oaks, New York, United States
View Trial DetailsNCT06035159
Anxiety, Anxiety Disorders
Ghent, Belgium
View Trial DetailsNCT05056454
Anxiety, Anxiety Disorders
Los Angeles, California, United States
View Trial DetailsNCT06520241
Anxiety, Anxiety Disorders
Bartın, Turkey (Türkiye)
View Trial Details