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

Primary Purpose

Maternal Depression

Status
Completed
Phase
Not Applicable
Locations
Pakistan
Study Type
Interventional
Intervention
LTP Plus
TAU
Sponsored by
Pakistan Institute of Living and Learning
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Maternal Depression

Eligibility Criteria

18 Years - 44 Years (Adult)FemaleDoes not accept healthy volunteers

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.

Sites / Locations

  • Pediatric units
  • Pedratric units
  • Pediatric units
  • Pediatric units
  • Pediatric units
  • Pediatric units

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

LTP Plus

Treatment as Usual (TAU)

Arm Description

LTP Plus group participants will receive intervention over the telephone for 3 months one session per week for 2 months and rest of the sessions fortnightly by trained graduates, expert in delivering LTP plus intervention.

TAU group will receive routine care and their follow up will be done after completion of the intervention and then at 6-month post randomization.

Outcomes

Primary Outcome Measures

Structured Clinical Interview for DSM-IV (SCID)
The primary outcome is depression which will be measured using Structured Clinical Interview for DSM-V Disorders (SCID)

Secondary Outcome Measures

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
The Postpartum Bonding Questionnaire (PBQ)
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'.
Experiences in Close Relationships-Revised (ECR-R)
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)
DAS is a 32 items self-report questionnaire, to measure couple satisfaction and to assess how each partner perceives his/her relationship.
Client Service Receipt Inventory
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.
Infant development: Infant development:
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 Questionnaire
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.
World Health Organisation Quality of Life (WHO, 2004)
A self-report scale comprising of 26 items which measures physical health, psychological health, social relationships and environment.
Learning Through Play (LTP) KAP Questionnaire
This scale will be used to measure change in Knowledge, Attitude and Practices (KAP) at different time points.
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. 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 Questionnaire
The participants will rate their satisfaction with treatment after completion of intervention. Higher score indicate greater satisfaction
How are you feeling scale
This is a pictorial scale to assess mood disturbance. higher score indicate greater severity of depression.

Full Information

First Posted
February 6, 2018
Last Updated
July 7, 2021
Sponsor
Pakistan Institute of Living and Learning
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1. Study Identification

Unique Protocol Identification Number
NCT03430622
Brief Title
Learning Through Play (LTP) Plus Interpersonal Psychotherapy (IPT)
Acronym
TLMC
Official Title
Telephone Delivered Learning Through Play (LTP) Plus Interpersonal Psychotherapy (IPT) for Depressed Mothers - A Multicentre Randomized Controlled Trial (RCT) in a Low-Income Country
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Completed
Study Start Date
February 20, 2018 (Actual)
Primary Completion Date
August 20, 2019 (Actual)
Study Completion Date
August 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Pakistan Institute of Living and Learning

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Maternal Depression

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
Researchers doing outcome assessment will be kept blind to the group allocations
Allocation
Randomized
Enrollment
370 (Actual)

8. Arms, Groups, and Interventions

Arm Title
LTP Plus
Arm Type
Experimental
Arm Description
LTP Plus group participants will receive intervention over the telephone for 3 months one session per week for 2 months and rest of the sessions fortnightly by trained graduates, expert in delivering LTP plus intervention.
Arm Title
Treatment as Usual (TAU)
Arm Type
Active Comparator
Arm Description
TAU group will receive routine care and their follow up will be done after completion of the intervention and then at 6-month post randomization.
Intervention Type
Behavioral
Intervention Name(s)
LTP Plus
Other Intervention Name(s)
Psycho-social Intervention
Intervention Description
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.
Intervention Type
Other
Intervention Name(s)
TAU
Other Intervention Name(s)
Treatment as Usual
Intervention Description
This group will be on their routine care and will not be given any intervention
Primary Outcome Measure Information:
Title
Structured Clinical Interview for DSM-IV (SCID)
Description
The primary outcome is depression which will be measured using Structured Clinical Interview for DSM-V Disorders (SCID)
Time Frame
Time Frame: Changes from baseline to 6th month after randomization ]
Secondary Outcome Measure Information:
Title
Generalized Anxiety Disorder (GAD) 7
Description
The GAD-7 is a 7 item scale will be used to screen for and measure severity of Generalized Anxiety Disorder
Time Frame
[Time Frame: Changes from baseline to 3rd month and 6th month after randomization]
Title
The Postpartum Bonding Questionnaire (PBQ)
Description
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'.
Time Frame
[Time Frame: Changes from baseline to 3rd month and 6th month after randomization]
Title
Experiences in Close Relationships-Revised (ECR-R)
Description
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.
Time Frame
[Time Frame: Changes from baseline to 3rd month and 6th month after randomization]
Title
Dyadic Adjustment Scale, (DAS)
Description
DAS is a 32 items self-report questionnaire, to measure couple satisfaction and to assess how each partner perceives his/her relationship.
Time Frame
[Time Frame: Changes from baseline to 3rd month and 6th month after randomization]
Title
Client Service Receipt Inventory
Description
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.
Time Frame
[Time Frame: Changes from baseline to 3rd month]
Title
Infant development: Infant development:
Description
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.
Time Frame
[Time Frame: Changes from baseline to 3rd month and 6th month after randomization]
Title
Ages and Stages Social-Emotional Questionnaire
Description
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.
Time Frame
Changes from baseline to 3rd month and 6th month after randomization]
Title
World Health Organisation Quality of Life (WHO, 2004)
Description
A self-report scale comprising of 26 items which measures physical health, psychological health, social relationships and environment.
Time Frame
Changes from baseline to 3rd month and 6th month after randomization]
Title
Learning Through Play (LTP) KAP Questionnaire
Description
This scale will be used to measure change in Knowledge, Attitude and Practices (KAP) at different time points.
Time Frame
Changes from baseline to 3rd month and 6th month after randomization]
Title
Patient Health Questionnaire (PHQ-9)
Description
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.
Time Frame
Time Frame: Changes from baseline to 3rd month and 6th month after randomization ]
Title
Client Satisfaction Questionnaire
Description
The participants will rate their satisfaction with treatment after completion of intervention. Higher score indicate greater satisfaction
Time Frame
Time Frame: Score at 3rd month assessment only.
Title
How are you feeling scale
Description
This is a pictorial scale to assess mood disturbance. higher score indicate greater severity of depression.
Time Frame
Time Frame: Changes from baseline to 3rd month and 6th month after randomization ]

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
44 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nasim Chaudhry
Organizational Affiliation
Pakistan Institute of Living & Learning
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pediatric units
City
Quetta
State/Province
Balochistan
Country
Pakistan
Facility Name
Pedratric units
City
Lahore
State/Province
Punjab
Country
Pakistan
Facility Name
Pediatric units
City
Hyderabad
State/Province
Sindh
Country
Pakistan
Facility Name
Pediatric units
City
Karachi
State/Province
Sindh
Country
Pakistan
Facility Name
Pediatric units
City
Nawabshah
State/Province
Sindh
Country
Pakistan
Facility Name
Pediatric units
City
Peshawar
State/Province
Sindh
Country
Pakistan

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

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

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