Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT04663243 |
Other study ID # |
THP in clinical settings |
Secondary ID |
|
Status |
Completed |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
July 3, 2020 |
Est. completion date |
April 29, 2021 |
Study information
Verified date |
September 2021 |
Source |
University of the Punjab |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
The trial is to evaluate the effect of an evidence-informed, depression focused early
prenatal prevention intervention at six weeks' postpartum. Secondary objective is to explore
demographical and psychosocial factors responsible for development of prenatal and postpartum
depression. Investigator will also examine the potential mediators of depression and the
effect of intervention on depression and its related factors i.e. marital relationship,
social support, empowerment and history of intimate partner violence. Pregnant women coming
for their antenatal visits to the Sheikh Zayed Hospital (SZH), a public facility in Lahore,
Pakistan, will be screened for eligibility. Eligible women will be 24-26 weeks pregnancy who
will be assessed as having mild to moderate levels of depression [i.e., score ≥10 on Personal
Health Care Questionnaire (PHQ-9)] validated in Pakistan for the use of non-specialist.
Description:
The present study aims to evaluate the effectiveness of evidence informed, depression focused
early prenatal prevention intervention in pregnant women at six weeks' postpartum.
Investigator hypothesize that women with subclinical to clinical levels of prenatal
depression to the intervention will result in fewer cases of depression (mild to moderate) at
six weeks' postpartum. The primary objective of the trial is to evaluate the effect of an
evidence-informed, depression focused early prenatal prevention intervention at six weeks'
postpartum. Secondary objective is to explore demographical and psychosocial factors
responsible for development of prenatal and postpartum depression. We will also examine the
potential mediators of depression and the effect of intervention on depression and its
related factors i.e. marital relationship, social support, empowerment and history of
intimate partner violence. Pregnant women coming for their antenatal visits to the Sheikh
Zayed Hospital (SZH), a public facility in Lahore, Pakistan, will be screened for
eligibility. Eligible women will be 24-26 weeks pregnancy who will be assessed as having mild
to moderate levels of depression [i.e., score ≥10 on Personal Health Care Questionnaire
(PHQ-9)] validated in Pakistan for the use of non-specialist.
An intervention thinking Healthy Program (THP) will be done in which Investigator will enroll
up to twenty (20) pregnant women. Low line psychosocial intervention based on the principles
of Cognitive Behavior Therapy (CBT), designed for non-specialist will be applied for
expectant women experiencing depression during mid to late-pregnancy. It uses the core
principles and strategies of the Thinking Healthy Program (THP), an evidence-based
psychosocial intervention for mothers experiencing perinatal depression, including empathetic
listening, thought challenging, behavior activation, family involvement, and problem
management. Additionally, stress management skills such as breathing exercises are
incorporated. Culturally relevant customized illustrations are used for guided discovery,
behavior activation, stress management, and to convey key health messages. The intervention
is a series of one-on-one sessions, complemented by take home exercises. Before and after
intervention comparison will be made to find out the efficacy of intervention. The data will
be collected at one site: Sheikh Zayed Hospital, a public tertiary care facility in Lahore,
Pakistan. It will take six months for data collection.