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Antenatal Relaxation Group for Anxiety and Depression Management

Antenatal Depression Group Research Project: The Effectiveness of Mindfulness-based Relaxation and Interpersonal Therapy to Relieve Anxiety and Depression Symptoms in Pregnant Women.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00855192
Acronym
ARG
Enrollment
20
Registered
2009-03-04
Start date
2008-10-31
Completion date
2009-12-31
Last updated
2010-03-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Depression

Keywords

anxiety, depression, pregnancy, antenatal, prenatal, mindfulness-based therapy, interpersonal therapy, support groups

Brief summary

Approximately 20% of pregnant women experience depression. Untreated depression during pregnancy is linked to decreased prenatal care, difficulties in the pregnancy, poorer outcomes for the baby, and developmental, language, and behaviour problems in the older child. While medication can often offer relief, pregnant women suffering with depression are often reluctant to take medications that may affect the unborn baby. There is little research about the effectiveness of other treatments such as support groups. The investigators project will provide relaxation groups for pregnant women with anxiety and depression. The group will provide a chance to get support from other pregnant women. Two health care specialists will provide information about anxiety and depression. They will also teach the skills for women to manage their symptoms. Women will be asked to complete a few questionnaires to evaluate their symptoms before, during, and after they join the group. They will also be asked to evaluate how the group met their needs.

Detailed description

Pregnant women between 15-28 weeks, who speak english are invited to join an 8 week group to relieve anxiety and depression. We have collected sociodemographic data, as well as social support, life events. Outcome measures are a decrease in anxiety and depression-as measured by the Edinburgh Postnatal Depression Scale, the Cambridge Worry Scale, and the STAI-Trait Scale.

Interventions

interpersonal and psycho-educational

psycho-educational

Sponsors

Royal University Hospital Foundation, Saskatoon, SK, Canada
CollaboratorUNKNOWN
University of Saskatchewan
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
16 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* 15 to 28 weeks pregnant and English speaking

Exclusion criteria

* Non-English speaking

Design outcomes

Primary

MeasureTime frame
Depression as measured by Edinburgh Postnatal Depression Scale and anxiety as measured by the State-Trait Anxiety Inventory and the Cambridge Worry ScaleParticipants will be asked to complete the questionnaires before the group commences, at 4 weeks, at the end of the group, and 6 weeks postpartum.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026