Development and Assessment of a Mobile Phone Based Intervention to Reduce Maternal Depression and Improve Child Health (TechMother)

Pakistan Institute of Living and Learning

Status

Completed

Conditions

Maternal Depression

Treatments

Behavioral: Mobile based intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT02526355

TechMotherCare001

Details and patient eligibility

About

The prevalence rate of maternal depression in Pakistani women and its effect on the growth and development of young children and child mortality is very high.

The main objective of this study is to increase access to evidence based psychological interventions for mothers who have children of age 0 to 30 months, consistent with her values. The study will be a 2 (conditions) into 3 (Time) single blind randomized controlled trail. Depressed mothers will be randomized either to intervention arm or control arm. Intervention will include text messages based on Learning Through Play Plus (LTP plus CBT).

Full description

Disturbances in mother-infant relationship in depressed mothers negatively influence the child's development. There are a number of efficient treatments for postnatal depression including antidepressant medication, psychotherapy and psychosocial interventions. Tele-health and mobile health is a novel and emerging field in psychiatric and psychological care and treatment of mental health difficulties, it involves the use of telecommunications to provide health care, support and intervention from a distance.

The proposed study will test the efficacy of an innovative, affordable mobile based intervention program that can help mothers with postnatal depression in low resource countries such as Pakistan.

Participants will be recruited from maternal and child care centres in Karachi, Pakistan and those participants (n = 204) meeting inclusion criteria of the study will be randomized into one of the 2 treatment arms, i.e., intervention or control, after completion of baseline assessment. Intervention will be comprised of LTP Plus and will be delivered through text messages. Momentary Sampling assessment and Momentary Psychological intervention will be part of this study. Participants will be assessed again after completion of intervention (i.e., after 12 weeks) and then 3 months post intervention.

Enrollment

208 patients

Sex

Female

Ages

18 to 44 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Mothers with mild to moderate depression will be included
Mother of children age 0-30months
The age range in the study is 18 to 44 years
Participants having mobile phones will be included

Exclusion criteria

Subjects will not be included if they had a diagnosed medical condition or significant physical or learning disability
Any form of psychosis, or are currently under psychiatric care.
Mothers with severe depression or suicidal ideation will not be included
Mothers who will be receiving any psychological intervention will be excluded
Mothers of children with any serious medical or psychiatric illness will also be excluded.