Behavior Disorders in Children Clinical Trial
Official title:
Effectiveness of Child-Parent Relationship Therapy (CPRT) for Management of Psychological Distress and Family Functioning Among Parents of Children Exposed to Trauma
Exposure to trauma during childhood contributes to behavioral and attachment difficulties in children. The current research study will be conducted on the effectiveness of child-parent relationship therapy (CPRT) on psychological distress and family functioning among parents of children exposed to trauma. The CPRT is an evidence-based intervention parenting program that gives training to the parents, to help children who have social, emotional, attachment, and behavioral difficulties. A CPRT would train parents with the principles of CCPT and provide them with the ability to support their children. A randomized controlled trial will validate the effect of CPRT on family functioning, and parental psychological distress among parents of children exposed to trauma. It will be an interventional-based study on CPRT with a pre-posttest experimental design. The current study would be conducted in Islamabad and Rawalpindi, after obtaining permission from the appropriate authorities, for collecting data from the educated mothers/caretakers as a research sample. There would be inclusive and exclusive selection criteria for the sample. A study will be conducted in four ways, firstly, the need assessment will be conducted with phenomenological research design from selected educated mothers/caretakers on the KAP model (knowledge, attitudes, and practices) categories about the CPRT, and psychological distress on family functioning among parents of children exposed to trauma. In phase two, the pilot study will be conducted to assess the accuracy of measures for the sample and the effectiveness of CPRT. In phase three, a cross-sectional survey would measure the study variables. The fourth phase will be the intervention phase for validation of CPRT therapeutic techniques in the Pakistani population a randomized controlled trial design will be applied to analyze the effect of CPRT on study variables in the next phase (main study). The measures Child-Parent Relationship Scale, depression, anxiety, and stress scale, family assessment device, and disruptive behavior through Children's Behavior Questionnaire (very short form) parental-version will be used to collection the data from study participants. The Child and Adolescent Trauma Screen would be used as a screening inventory. The CPRT intervention therapeutic sessions will continue based on the inclusive and exclusive selection criteria. The data will be evaluated through SPSS (latest version).
Status | Recruiting |
Enrollment | 60 |
Est. completion date | March 9, 2024 |
Est. primary completion date | December 31, 2023 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 20 Years to 55 Years |
Eligibility | Inclusion Criteria: 1. qualification would be graduation minimum and above 2. location: from Pakistan's twin cities (Rawalpindi and Islamabad). 3. the parents of children exposed to traumatic experiences - child abuse (physical abuse, yelling, Psychological Abuse) - bullying, (witness of bullying, verbal bullying, physical bullying) - fighting, (street fighting. witness of fighting) - traumatized grief, (death of a loved one) - Robbery and - parents' separation. Exclusion Criteria: Exclusive Sample criteria - uneducated parents, (less then graduation) - domestic violence - child sexual abuse, - natural disasters, - traumatic events that caused physical disabilities, - war, - terrorism victims, and - families who would be taking any psychotherapy or training to manage psychological distress and child disruptive behavior. |
Country | Name | City | State |
---|---|---|---|
Pakistan | Tayyaba Hanif | Rawalpindi |
Lead Sponsor | Collaborator |
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Fatima Jinnah Women University |
Pakistan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Child and Adolescent Trauma Screen-Caregiver | The questionnaire is indeed a screening tool designed to assess potentially traumatic events and posttraumatic stress symptoms (PTSS) in children and adolescents. It is based on the DSM-5 criteria for PTSD. The CATS questionnaire typically consists of questions related to traumatic events and symptoms associated with PTSD. According to the DSM-5, (2013) the CATS measures potentially traumatic experiences and posttraumatic stress symptoms (PTSS). age 3-17 y | 5-10 minutes | |
Primary | Child Parent Relationship Scale | it consists of fifteen items about the child and the parent's relationship with it. Likert weighed the fifteen items on a 5-point scale, and CPRS can be summarized by groups of objects that most closely correspond to the discrepancy and closeness. | 10-15 minutes | |
Primary | Depression Anxiety Stress Scale-42 | it is based on measurements rather than categorical concepts of mental distress, and scores emphasize symptoms are experienced, not diagnostic thresholds. it has been unable to use a child's scale for 12 years, The three symptom clusters are as follows: Depression: Illegal problems, despair, life assessment, vertical, pride, interest/involvement, and tribe/involvement, Anxiety: Herbal arousal, skeletal muscle effects, conditional warnings, fear of anxiety. Stress: Chronic non-special Here, the complexity is comfortable, nervous, easily frustrated/excited, sensitive/impatient beyond. | 5-10 minutes | |
Primary | Family Assessment Device | measures structural, organizational, and transactional factors within families. A total of six scales are used to measure the six dimensions of the MMFF - affective involvement, affective responsiveness, behavioral control, communication, problem solving, and roles - as well as a seventh measure measuring general family functioning | 10-15 minutes | |
Secondary | Child and adolescent Behavior Inventory | A children's behavior questionnaire was used to assess the child's behavior. There were 75 items with 3-point Likert scale and evaluation for last 6 months.. it is suitable for the age range of the child between 6-17 years. | 5-10 minutes |
Status | Clinical Trial | Phase | |
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Completed |
NCT03353129 -
Adaptive Care in the Perioperative Setting
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