Evaluating the Efficacy of a Group Social Skills Intervention

Sponsor
The Hospital for Sick Children (Other)
Overall Status
Completed
CT.gov ID
NCT02677142
Collaborator
(none)
95
3
2
44
31.7
0.7

Study Details

Study Description

Brief Summary

Tumours affecting the brain are a very heterogeneous group of diseases. Accordingly, treatment strategies vary widely depending on child's age, tumour location, its resectability and histology. As a group, however, the survival rate of childhood brain tumors has improved in recent years, resulting in an increased number of survivors returning to school and reintegrating into their communities. Survival for many of them, however, has also come with severe costs such as neurocognitive and academic difficulties. Cognitive rehabilitation strategies to address these deficits have been a major focus of recent research. Evidence is now also mounting for social competence deficits among this population which may persist into late adolescence and adulthood, thereby negatively affecting long-term survivorship. Thus, there is an urgency to identify psychosocial interventions, such as social skills programs, that can reduce the social competence deficits in childhood brain tumor survivors and, therefore, modify the course of these outcomes to ensure that survivors thrive and become productive members of society. To date, no rigorous social skills intervention trials have been undertaken to address the social difficulties of these survivors. The current proposal is the first study that aims to address this gap by evaluating the efficacy of an innovative, manualized, social skills intervention program developed for this population using a multi-centre Randomized Control Trial (RCT).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Structured social skills training program, SSIP
  • Behavioral: CG - social skills activities
N/A

Detailed Description

Children and adolescents who are treated for brain tumours are faced with a variety of problems that affect the way they live their lives: one of the biggest problems is limited contact with friends and peers. This study aims to help kids and teens deal with this problem. The purpose of this study is to give kids who are treated for brain tumors opportunities to meet with other kids with similar experiences by participating in one of two social skills groups to improve how they related to one another. Investigators are assessing if these programs are beneficial to kids who have had brain tumours and which group is best. Kids will be assigned randomly to one of two groups. In both groups kids will meet with the other participants and with the facilitators for two hours once a week for 8 weeks. Kids in both groups will have introductions, group rules and group purpose (learn to relate with one another) through fun with games and arts and crafts. In one group, the games and crafts will be used for learning social skills. In the other group, arts and crafts and playing will be the focus of the activities, with the goal for each session determined by creating a craft or playing a game where everyone can win. One parent and all kids will complete questionnaires before the group starts, after the last group session as well as 6 months following the group. The questionnaires will ask questions about feeling, actions and getting along with others. Investigators also plan to visit the child's school so that the child, classmates and teachers will fill out questionnaires about friendships.

Study Design

Study Type:
Interventional
Actual Enrollment :
95 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
A Randomized Control Trial to Evaluate the Efficacy of a Group Social Skills Intervention for Childhood Survivors of Brain Tumours
Study Start Date :
Apr 1, 2012
Actual Primary Completion Date :
Dec 1, 2015
Actual Study Completion Date :
Dec 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Attention Control Group (CG)

Behavioural: CG: Social Skills Activities: Participants in this arm will experience an 8-week manualized intervention program with activities and games. Sessions will NOT be designed around a specific social skill and activities and games will NOT have a specific focus. Sessions will be conducted by facilitators who will receive the standard training for volunteers and will work under the supervision of one of the investigators at each site.

Behavioral: CG - social skills activities
Sessions will not be designed around a specific social skill and activities and games will not have a specific focus. CG sessions will be conducted by facilitators who will receive the standard training for volunteers and will work under the supervision of one of the investigators at each site.

Experimental: Experimental Group (EG)

Behavioral: Structured social skills training program, SSIP. Participants in this arm will experience an 8-week manualized intervention program that addresses six major social skills, one per session, starting with easier skills (Social Initiation and Friendship Making, Cooperation) and moving towards more complex skills (Managing Teasing and Bullying, Conflict Resolution, Empathy, and Assertion). Sessions will be conducted by facilitators who will receive the standard training for volunteers and will work under the supervision of one of the investigators at each site.

Behavioral: Structured social skills training program, SSIP
Detailed, session by session, in the manual written for this purpose. It addresses six major social skills, one per session, starting with easier skills (Social Initiation and Friendship Making, Cooperation) and moving towards more complex skills (Managing Teasing and Bullying, Conflict Resolution, Empathy, and Assertion).

Outcome Measures

Primary Outcome Measures

  1. Parent-rated social skills - assessment of change across three time points [day 1, 8 weeks later, and 6 months after day 1]

    Measured by Social Skills Rating System (SSRS)[37]. The SSRS is a standardized instrument that has parent, teacher and child versions.

  2. Child-rated social skills -- assessment of change across three time points [day 1, 8 weeks later, and 6 months after day 1]

    Measured by Social Skills Rating System (SSRS)[37]. The SSRS is a standardized instrument that has parent, teacher and child versions.

Secondary Outcome Measures

  1. Quality of life ratings - general, parental assessment of change across three time points [day 1, 8 weeks later, and 6 months after day 1]

    Quality of Life Inventory - PedsQL, generic[38] - Parent report

  2. Quality of life ratings - general, child assessment of change across three time points [day 1, 8 weeks later, and 6 months after day 1]

    Quality of Life Inventory - PedsQL, generic[38] - Child self-report

  3. Quality of life ratings - brain tumour module, parent assessment of change across three time points [day 1, 8 weeks later, and 6 months after day 1]

    Quality of Life Inventory - PedsQL, Brain Tumour Module[38] - parent report

  4. Quality of life ratings - brain tumour module, child assessment of change across three time points [day 1, 8 weeks later, and 6 months after day 1]

    Quality of Life Inventory - PedsQL, Brain Tumour Module[38] - Child self-report

  5. Child's social functioning - assessment of change across three time points [day 1, 8 weeks later, and 6 months after day 1]

    subscale of the Behavior Assessment System for Children-Second Edition, BASC-2, completed by parents

Eligibility Criteria

Criteria

Ages Eligible for Study:
8 Years to 16 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Diagnosed with a brain/spinal tumour

  2. off treatment for at least 3 months or on maintenance chemotherapy but medically stable, e.g., low grade gliomas

  3. between 8 and 16 years of age at the time of enrollment

  4. have sufficient fluency in English for active group participation

  5. attending school regularly and in a regular classroom for at least 50% of a school day

Exclusion Criteria:
  1. Severe cognitive deficits, as defined by enrollment in full-time special classroom, which will prevent them from participating fully

  2. a diagnosis of conduct disorder or any other condition that may interfere with group activities. Survivors and parents who have some difficulties reading (i.e., English is their second language) will be assisted by a research assistant (RA) in completing the questionnaires.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Alberta Childrens Hospital Calgary Alberta Canada
2 BC Women and Children's Hospital Vancouver British Columbia Canada
3 The Hospital for Sick Children Toronto Ontario Canada M5V1X8

Sponsors and Collaborators

  • The Hospital for Sick Children

Investigators

  • Principal Investigator: Maru Barrera, MD, The Hospital for Sick Children

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Maru Barrera, Psychologist, The Hospital for Sick Children
ClinicalTrials.gov Identifier:
NCT02677142
Other Study ID Numbers:
  • 1000014297
First Posted:
Feb 9, 2016
Last Update Posted:
May 9, 2016
Last Verified:
May 1, 2016
Keywords provided by Maru Barrera, Psychologist, The Hospital for Sick Children
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 9, 2016