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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03379077
Other study ID # PILL-ROSHNI2
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 20, 2017
Est. completion date February 28, 2019

Study information

Verified date April 2022
Source Pakistan Institute of Living and Learning
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study has both quantitative and qualitative components. The objective of the quantitative study is to: Determine if supported implementation of the LTP plus programme improves infant development compared to standard implementation of the LTP plus programme. The objective of the qualitative study is: Process evaluation and finding out about implementation challenges (from the perspective of the mothers and the people delivering both the LTP plus and the supported implementation intervention).


Description:

In Pakistan, the Learning through Play parenting program was tested initially through a cluster randomized study in a rural area of Pakistan. The results of this recently completed cluster RCT funded by the Grand Challenges Canada (GCC) showed that LTP Plus works and benefits both the mother and the child. More specifically, the results indicate a significant reduction in maternal depression. Purpose of this cluster RCT is to determine if supported implementation of the LTP plus programme improves infant development compared to standard implementation of the LTP plus programme. This is an implementation trial comparing two ways of introducing LTP plus. A Cluster RCT of culturally adapted intervention LTP Plus will be conducted in the villages of Gadap town, Karachi, Pakistan. Total 60 villages will be randomized in two groups LTP plus and LTP plus supported implementation. Each cluster will be made of up to 15 mothers. Participants will be screened using eligibility checklist. Assessments will be done at baseline and after completion of intervention (3-month). All follow ups will be done by independent RAs, not involved in delivering intervention sessions.


Recruitment information / eligibility

Status Completed
Enrollment 1006
Est. completion date February 28, 2019
Est. primary completion date February 28, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 44 Years
Eligibility Inclusion Criteria: Participants will be included in the study if they are: 18 to 44 years old mothers with children aged between 0-33 months, resident in the trial site catchments area, who are able to complete assessments Exclusion Criteria: Participants will be excluded from the study if they have: A medical disorder that would prevent participation in clinical trial. Temporary resident unlikely to be available for follow up. Active suicidal ideation or any other severe or physical mental disorder.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
LTP Plus
LTP Plus is comprised of two components; Learning through play (LTP) and Cognitive Behavior Therapy (CBT). 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 Thinking Healthy Program (THP) which adopts 'here and now' problem-solving approach. THP uses cognitive behavior therapy (CBT) techniques of active listening, changing negative thinking, and collaboration with the family.

Locations

Country Name City State
Pakistan Gadap Karachi Sindh

Sponsors (3)

Lead Sponsor Collaborator
Pakistan Institute of Living and Learning Health and Nutrition Development Society, Hincks Dellcrest Centre

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Other Patient Health Questionnaire (PHQ) The Patient health Questionnaire (PHQ) is a simple 10 item self-report questionnaire will also be administered by a trained research worker. A score of 10 or more is taken as cut -off for depressive disorder, however all mothers meeting eligibility criteria will be included, despite their scores on PHQ-9. Baseline and 3rd Month
Other Generalized Anxiety Disorder (GAD) 7 The GAD-7 is a 7 item scale will be used to screen for and measure severity of Generalized Anxiety Disorder Baseline and 3rd Month
Other Knowledge of Expectation and Child Development A 25-item questionnaire will be used to assess maternal knowledge and expectations for child development in the first three years Baseline and 3rd Month
Other Parenting Stress Index - Short Form Parents rate 36 items on a five-point scale (1-5) on three scales: (1) Parenting Distress, (2) Difficult Child Characteristics, and (3) Dysfunctional Parent-Child Interaction. Baseline and 3rd Month
Other Multidimensional Scale of Perceived Social Support (MSPSS) This brief scale will be used to measure social support Baseline and 3rd Month
Other Euro-Qol-5 Dimensions (EQ-5D) Health-related quality of life will be measured using the EQ-5D Baseline and 3rd Month
Other Client Service Receipt Inventory We will collect information about the use of other health services (including the informal sector faith healers/Imams) using CSRI. Baseline and 3rd month
Other CSQ Client Satisfaction Questionnaire The participants will rate their satisfaction with treatment after completion of intervention using the CSQ. 3rd Month
Primary Infant development: Ages and Stages Questionnaire (Squires, Bricker, & Twombly, 2009) This scale will be used to measure child development. Parents will report on their child's communication,gross motor, fine motor, problem solving and personal-social development. Change from baseline at 3rd Month
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