NCT06178705

Brief Summary

The main objectives of the study are:

  1. 1.To find out the effectiveness of Helpful Parenting Program (HPP) for psychological functioning of children's parent having behavioral and emotional issues.
  2. 2.To decrease psychological distress among children's parent having behavioral and emotional issues.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
200

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Nov 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 15, 2023

Completed
14 days until next milestone

First Submitted

Initial submission to the registry

November 29, 2023

Completed
22 days until next milestone

First Posted

Study publicly available on registry

December 21, 2023

Completed
11 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2024

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 10, 2024

Completed
Last Updated

December 21, 2023

Status Verified

December 1, 2023

Enrollment Period

2 months

First QC Date

November 29, 2023

Last Update Submit

December 19, 2023

Conditions

Keywords

HPP, Parenting, Emotional & behavioral issues

Outcome Measures

Primary Outcomes (3)

  • Strength and difficulty questionnaire

    This scale will assess the parents strength and difficulty dealing the child

    4 months

  • Depression Anxiety and Stress Scale

    This scale will assess the level of depression, anxiety and stress among the parents of emotionally disturbed child

    4 months

  • Dyadic Adjustment Scale

    This scale will assess the parents level of adjustment

    4 months

Secondary Outcomes (2)

  • Parenting Scale

    4 months

  • Parents sense of competence scale

    4 months

Study Arms (2)

Treatment Group

EXPERIMENTAL

Experimental Group: Participants in experimental group would receive 8-10 sessions of intervention based helpful parenting program

Behavioral: Helpful Parenting Program Intervention

Control Group

NO INTERVENTION

Control Group: Participants in the control group will not receive the said intervention of helpful parenting program.

Interventions

8-10 sessions with 60 minutes duration once in a week will be conducted with the parents in group and one-on-one setting. Helpful parenting program would be based on social learning theory, behavior modification and couple counseling. The program will be used as an intervention strategy with parents to built insight about their child's emotional \& behavioral issues. Different strategies to teach parenting skills will also be used as an intervention. Further more, this program will target parents' psychological distress and couples' problematic conflicts regarding parenting

Treatment Group

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Only parents with dysfunctional parenting practices, having children with emotional and behavioral issues would be a part of the study. Second, Only parents would be included in the study who score above 18 on SDQ-4. Only parents having children aged 5 to 12 years would be included in the study. The participants would be taken from any socioeconomic status.

You may not qualify if:

  • Parents with major psychological disorders would be excluded from the study. The parent served as single parent would be excluded from the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Qasir Abbas

Faisalabad, Punjab Province, 38000, Pakistan

Location

Study Officials

  • Qasir Abbas, PHD

    Government College University Faisalabad

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Randomized control trial design would be used in this study which is two arm study having two groups, an experimental \& wait-list control group. Experimental group will receive intervention while other group will be placed in wait-list. In this study, parallel group design would be used. The treatment will be given to all participants in a parallel way. Allocation ratio and framework would be equivalence i.e., equal number of participants in treatment and control group.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr. Qasir Abbas Assistant Professor Clinical Psychology

Study Record Dates

First Submitted

November 29, 2023

First Posted

December 21, 2023

Study Start

November 15, 2023

Primary Completion

January 1, 2024

Study Completion

April 10, 2024

Last Updated

December 21, 2023

Record last verified: 2023-12

Data Sharing

IPD Sharing
Will not share

Locations