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Learning Through Play (LTP) Plus Interpersonal Psychotherapy (IPT)

Telephone Delivered Learning Through Play (LTP) Plus Interpersonal Psychotherapy (IPT) for Depressed Mothers - A Multicentre Randomized Controlled Trial (RCT) in a Low-Income Country

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03430622
Acronym
TLMC
Enrollment
370
Registered
2018-02-13
Start date
2018-02-20
Completion date
2019-08-30
Last updated
2021-07-13

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

Conditions

Maternal Depression

Brief summary

To evaluate the effectiveness of a telephone based LTP Plus intervention for maternal depression.

Detailed description

Despite the high prevalence of maternal depression in Pakistan, research on psychosocial interventions is limited. We will test the effectiveness of a telephone based intervention program called Learning through Play plus Interpersonal Psychotherapy (LTP Plus) that can be used by non-specialists, including trained graduates, mothers and lay health workers with minimal training. This telephone communication will be supplemented by the provision of LTP Plus pictorial calendars to the depressed mothers. Purpose of this RCT is to determine if telephone delivered intervention of the LTP plus programme reduces symptoms of maternal depression and improves infant development compared to Treatment as usual. A sample of 354 (177 in each group) will be required. The study will be conducted in big cities of Pakistan including Karachi, Lahore, Hyderabad, Nawabshah, Quetta and Peshawar.Participants will be screened using Patient Health Questionnaire (PHQ-9) and eligibility checklist. Those scoring 10 and above on PHQ-9 will be invited to participate in the study. Assessments will be done at baseline and after completion of intervention (3rd month and 6th month after randomization). All follow ups will be done by independent Research Assistants (RAs), blind to the treatment allocations.

Interventions

BEHAVIORALLTP Plus

LTP Plus is comprised of two components; Learning through play (LTP) and Interpersonal Psychotherapy (IPT). The LTP Plus is a low-literacy; sustainable program intended to provide parents with information on the healthy growth and development of their young children. The LTP research-based activities enhance children's development while simultaneously promoting attachment security through building parents' ability to read and be sensitive to their children's cues and through active involvement in their children's development. Plus the Interpersonal Psychotherapy (IPT) intervention is comprised of a supportive element, an educational element, a parenting element and an interpersonal relationship element. Intervention goals include helping mothers feel supported, empowered and confident about their parenting abilities, which would directly influence reduction in depressive symptoms as well as resolution of interpersonal conflicts.

OTHERTAU

This group will be on their routine care and will not be given any intervention

Sponsors

Pakistan Institute of Living and Learning
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Researchers doing outcome assessment will be kept blind to the group allocations

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 44 Years
Healthy volunteers
No

Inclusion criteria

Participants will be included in the study if they are: 18 to 44 years old mothers with children aged between 0-30 months having a diagnosis of major depressive disorder using the Structure Clinical Interview for DSM-V, Ability to complete a baseline assessment, Participating mother having telephone/mobile phone access for at least one hour per week.

Exclusion criteria

Participants will be excluded from the study if they have: Any medical illness that will prevent them from participation in the clinical trial, current or past diagnosis of bipolar depression, currently using antidepressants or receiving any kind of psychotherapy, active suicidal ideation, any other severe physical or mental disorder, no access to telephone/mobile.

Design outcomes

Primary

MeasureTime frameDescription
Structured Clinical Interview for DSM-IV (SCID)Time Frame: Changes from baseline to 6th month after randomization ]The primary outcome is depression which will be measured using Structured Clinical Interview for DSM-V Disorders (SCID)

Secondary

MeasureTime frameDescription
World Health Organisation Quality of Life (WHO, 2004)Changes from baseline to 3rd month and 6th month after randomization]A self-report scale comprising of 26 items which measures physical health, psychological health, social relationships and environment.
Learning Through Play (LTP) KAP QuestionnaireChanges from baseline to 3rd month and 6th month after randomization]This scale will be used to measure change in Knowledge, Attitude and Practices (KAP) at different time points.
Infant development: Infant development:[Time Frame: Changes from baseline to 3rd month and 6th month after randomization]Ages and Stages Questionnaire will be used to measure child development. Parents will report on their child's communication, gross and fine motor skills, problem solving and personal-social development at different time points.
Ages and Stages Social-Emotional QuestionnaireChanges from baseline to 3rd month and 6th month after randomization]Ages and Stages will be used to obtain maternal report on their child's social and emotional development. The questionnaire is already translated in Urdu and will be used in the proposed trial.
Generalized Anxiety Disorder (GAD) 7[Time Frame: Changes from baseline to 3rd month and 6th month after randomization]The GAD-7 is a 7 item scale will be used to screen for and measure severity of Generalized Anxiety Disorder
Client Service Receipt Inventory[Time Frame: Changes from baseline to 3rd month]We will collect information about the use of other health services (including the informal sector, faith healers/Imams) using CSRI based on our previous work in Pakistan.
Experiences in Close Relationships-Revised (ECR-R)[Time Frame: Changes from baseline to 3rd month and 6th month after randomization]The ECR-R measures individuals on two subscales of attachment: Avoidance and Anxiety. In general avoidant individuals find discomfort with intimacy and seek independence, whereas anxious individuals tend to fear rejection and abandonment.
Dyadic Adjustment Scale, (DAS)[Time Frame: Changes from baseline to 3rd month and 6th month after randomization]DAS is a 32 items self-report questionnaire, to measure couple satisfaction and to assess how each partner perceives his/her relationship.
Patient Health Questionnaire (PHQ-9)Time Frame: Changes from baseline to 3rd month and 6th month after randomization ]The Patient health Questionnaire (PHQ-9) is 9 items self-report questionnaire. A score of 10 or above is taken as cut -off point for depressive disorder. This scale will be used to check severity of depression. Patient Health Questionnaire (PHQ-9) The Patient health Questionnaire (PHQ-9) is 9 items self-report questionnaire. A score of 10 or above is taken as cut -off point for depressive disorder. This scale will be used to check severity of depression.
Client Satisfaction QuestionnaireTime Frame: Score at 3rd month assessment only.The participants will rate their satisfaction with treatment after completion of intervention. Higher score indicate greater satisfaction
How are you feeling scaleTime Frame: Changes from baseline to 3rd month and 6th month after randomization ]This is a pictorial scale to assess mood disturbance. higher score indicate greater severity of depression.
The Postpartum Bonding Questionnaire (PBQ)[Time Frame: Changes from baseline to 3rd month and 6th month after randomization]The PBQ is designed to detect disturbance in the mother-child relationship. The scale has 25 items, each followed by six alternative responses ranging from 'always' to 'never'.

Countries

Pakistan

Outcome results

None listed

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