Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03135119
Other study ID # STUDY00006612
Secondary ID R21HD091887
Status Completed
Phase N/A
First received
Last updated
Start date November 15, 2017
Est. completion date March 18, 2020

Study information

Verified date May 2022
Source Milton S. Hershey Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will examine the incremental benefit of animal-assisted therapy (AAT) as an adjunct intervention when combined with Trauma-Focused Cognitive-Behavioral Therapy (TF-CBT) for the treatment of maltreated youth. In addition, the development of therapeutic rapport and the intensity of stress experienced during treatment sessions will be examined as mediational mechanisms of treatment outcome. This project will help determine whether a larger study to test the beneficial effects of AAT for maltreated youth is feasible and warranted.


Description:

The eventual goal of this line of research is to determine whether, and through what mechanisms, Animal-Assisted Therapy (AAT) is beneficial for the treatment of maltreated youth. The current project is a feasibility study to determine if larger clinical trials are warranted. The specific aims of the current study are (1) to examine whether the integration of AAT into standard Trauma-Focused Cognitive-Behavioral Therapy (TF-CBT) enhances treatment effectiveness, (2) to evaluate the tolerability and feasibility of AAT when integrated into TF-CBT, and (3) to evaluate hypothesized mediational processes that may explain observed positive effects for the integration of AAT. Maltreated youth may display myriad emotional and behavioral symptoms; prominent among these is posttraumatic stress (PTS). TF-CBT is a well-established evidence-based treatment for PTS and other symptoms subsequent to child maltreatment and, therefore, is a suitable intervention for this trial. Sixty (60) maltreated youth (ages 6-17) displaying elevated PTS will be assigned to receive TF-CBT or TF-CBT+AAT using a blocked randomization procedure. The TF-CBT protocol is the standard twelve 90-minute sessions typically used in research trials. Youth in the TF-CBT+AAT condition will receive the standard protocol with a certified service dog present in the room for each session and the youth will be allowed to interact with the dog during session. A pre-post design will be used to ascertain whether the addition of AAT prompts greater PTS reduction as well as greater improvements in other outcomes, including internalizing symptoms, externalizing symptoms, and emotion regulation. Outcome metrics include caregiver and youth-reported objective measures, and respiratory sinus arrhythmia (RSA) assessed via an electrocardiogram (ECG) during both a resting and stress reactivity paradigm. Feasibility metrics assessed include treatment satisfaction, ability to implement the TF-CBT techniques with a dog in the room, treatment disrupting events attributable to the dogs, and whether the dogs experience significant stress as a result of their participation. Stress experienced by the dog will be determined through RSA, salivary cortisol, and behavioral responses. Two prominent hypotheses regarding the mechanism of effect for AAT will be examined. First, therapeutic rapport will be assessed at multiple increments to determine whether the presence of the dog improved the quality or efficiency of development of rapport. Second, RSA will be recorded for the youth during treatment sessions to determine if the presence of the dog yielded a lower intensity of stress during the sessions. Both therapeutic rapport and level of in-session stress will be examined as mediating variables to determine whether either explained enhanced treatment outcomes. To improve the methodological rigor of the study, data will be collected by research assistants blinded to the youth's treatment condition and the same clinicians will implement both treatment conditions, thereby eliminating clinician-specific effects on outcomes.


Recruitment information / eligibility

Status Completed
Enrollment 33
Est. completion date March 18, 2020
Est. primary completion date March 18, 2020
Accepts healthy volunteers No
Gender All
Age group 6 Years to 17 Years
Eligibility Inclusion Criteria: - A caregiver willing to participate with the youth - An allegation of child maltreatment investigated by child protective services (CPS) or the police - A raw score of = 39 (borderline or clinical elevation) on the caregiver- report version of the UCLA PTSD Reaction Index for the DSM-5. Exclusion Criteria: - Severe developmental delays and/or psychiatric problems that necessitate a higher level of care for the child. An allegation of child maltreatment investigated by child protective services (CPS) or the police - Intellectual deficits for the child (IQ < 80 on a cognitive screener) - Caregiver inability to complete assessment measures due to psychiatric, cognitive, or other limitation - The available caregiver is suspected or known to have perpetrated maltreatment - A fear of dogs, a dog allergy, or any prior history of aggression toward animals for the child and/or caregiver

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
TF-CBT
TF-CBT is typically described as including 3 phases, each focusing on a common goal and encompassing a third of treatment (4 sessions). The first phase focuses on skills-building and includes psychoeducation, parenting skills training, relaxation skills training, affect modulation skills training, and cognitive coping skills training. The second phase involves focused gradual exposure activities, including construction of a narrative account of the child's maltreatment experiences and cognitive processing of maladaptive thoughts. The third phase emphasizes the child's mastery over environmental reminders of the maltreatment and includes sharing the trauma narrative with the caregiver, in vivo exposure to physical stimuli, and enhancing future development.
TF-CBT+AAT
TF-CBT, as described in the other arm, with animal-assisted therapy as an adjunct intervention. During the administration of TF-CBT, a certified service dog will be in the room and the participant may elect to interact with the dog as various points throughout the sessions.

Locations

Country Name City State
United States Penn State Hershey Medical Center-TLC Research and Treatment Center Harrisburg Pennsylvania

Sponsors (2)

Lead Sponsor Collaborator
Milton S. Hershey Medical Center Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Scores on the UCLA Posttraumatic Stress Disorder Reaction Index This is a caregiver version of the measure designed to assess child/youth posttraumatic stress disorder (PTSD) symptoms. This is a 27-item questionnaire were the frequency of each item is reported using a scale ranging from 0 (Never) to 4 (Most Days), yielding a potential full scale score ranging from 0 to 108. For inclusion in this study, a score of at least 32 on the pre-treatment administration was required as this score denotes the "borderline" range for the measure. Lower scores indicate fewer PTSD symptoms are present. Data were obtained at pre-treatment and every four weeks thereafter until the protocol was completed, **up to 13 weeks**. The last assessment completed, excluding the pre-treatment assessment, was considered post-treatment.
Secondary Change in Scores on the Strengths and Difficulties Questionnaire Emotional Symptoms Subscale The Strengths and Difficulties Questionnaire (SDQ) is a measure assessing the caregiver's observation of assorted emotional and behavioral concerns. This study utilized the "Emotional Symptoms" subscale, which collectively assesses symptoms of depression and anxiety. The subscale includes 5 items, each scored on a scale ranging from 0 (Never) to 2 (Certainly True). This results in possible total scores ranging from 0 to 10 with higher scores indicating a greater level of concern. Data were obtained at pre-treatment and every four weeks thereafter until the protocol was completed, **up to 13 weeks**. The last assessment completed, excluding the pre-treatment assessment, was considered post-treatment.
Secondary Change in Scores on the Screen for Child Anxiety Related Disorders The Screen for Child Anxiety Related Disorders (SCARED) is a 41-item measure where the youth self-reports on concerns related to various forms of anxiety. Answer options range from 0 (Not True or Hardly Ever True) to 2 (Very Often or Very True), resulting in a possible total score between 0 and 82 with higher scores indicating greater concerns. Data were obtained at pre-treatment and every four weeks thereafter until the protocol was completed, **up to 13 weeks**. The last assessment completed, excluding the pre-treatment assessment, was considered post-treatment.
Secondary Change in Scores on the Moods and Feelings Questionnaire The Moods and Feelings Questionnaire (MFQ) is a 13-item measure that asks youth to report their own concerns with depression-related symptoms. Each item is answered with a 0 (Not True), 1 (Sometimes Ture), or 2 (True). The items are summed to create a total score that may range from 0 to 26, with higher scores denoting a greater level of depressive symptoms. . Data were obtained at pre-treatment and every four weeks thereafter until the protocol was completed, **up to 13 weeks**. The last assessment completed, excluding the pre-treatment assessment, was considered post-treatment.
See also
  Status Clinical Trial Phase
Completed NCT00595010 - Effectiveness of a Multi-Component Evidence-Based Parent Training Program in Reducing Child Maltreatment Phase 1
Completed NCT00494286 - Abuse-Focused Cognitive Behavioral Therapy for Children Who Have Been Physically Abused Phase 1
Completed NCT03956628 - Evaluation of Preventive (Stay Safe) Training Program of Child Abuse for Teachers and Children N/A
Completed NCT04257331 - Parent Training to Reduce Behavioral Problems in Children With Autism Spectrum Disorder in China N/A
Recruiting NCT03198429 - Cluster RCT of Embedded Parenting Intervention to Prevent Recurrence and Reduce Impairment in Young Children Exposed to Domestic Violence N/A
Completed NCT03185728 - iLook Out for Child Abuse: An Innovative Learning Module for Childcare Providers N/A
Completed NCT02415933 - Child Protective Outcomes Among Ultra-poor Families in Burkina Faso N/A
Recruiting NCT06100679 - Responsible Engaged and Loving (REAL) Fathers Intervention Evaluation N/A
Completed NCT04160013 - Mitigating ACEs in Pediatric Primary Care: Cohort #2 With 6-24 Month Old Children N/A
Active, not recruiting NCT05729945 - Catholic Health Initiatives (CHI) St. Joseph's Children Home Visiting Longitudinal Study N/A
Completed NCT03305458 - Improving Quality of Care in Child Mental Health Service Settings N/A
Completed NCT04700696 - Enhancing Permanency in Children and Families N/A
Active, not recruiting NCT05479734 - Promoting Resilience and Lowering Risk in Early Childhood N/A
Completed NCT04163549 - Evaluating the Effectiveness of the Safe at Home Program N/A
Recruiting NCT04290234 - Childhood Trauma and Escape Decision Dynamics
Recruiting NCT04637581 - Wraparound for High-risk Families With Substance Use Disorders: Examining Family, Child, and Parent Outcomes N/A
Not yet recruiting NCT03745573 - Preventing Violence Against Children in Schools Study N/A
Active, not recruiting NCT04163367 - A Randomized Controlled Study of Safer Kids: A Manualized Intervention to Prevent Child Abuse N/A
Completed NCT04117971 - Knowledge, Attitude and Practice of Child Abuse Diagnosis and Reporting Among a Group of Egyptian Dentists
Recruiting NCT02225301 - iLookOut for Child Abuse -Online Learning Module for Early Childcare Providers N/A