Oxford Centre for Children and Young People in Pain
Oxford, Oxfordshire, United Kingdom
NCT Number: NCT04261114
The primary aim is to explore what it is about the experience of chronic pain that may cause emotional distress in some young people but not in others, and how particular individual characteristics, as well as family factors may contribute to young persons' pain experiences and their emotional responses to pain.
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Notify Me12 year–19 year
All sexes
Observational
Oxford, Oxfordshire, United Kingdom
This is a three-part observational follow-up study:
Part one will explore (a) whether the current sample reports emotional distress, including feelings of burdensomeness, hopelessness and thoughts and acts of self-harm, and if young people perceive there to be a link between pain and any such feelings of distress, and (b) which aspects of the pain experience, if any, are associated with such distress, using qualitative and quantitative data.
Part two will explore potential individual-level and family-level risk and resilience factors underpinning the hypothesised relationship between aspects of the pain experience and burdensomeness, hopelessness and thoughts and acts of self-harm, using adolescent and parental baseline data.
In part three, adolescent participants will be invited to complete daily diaries on their pain experience, three times per day over 7 days, in order to investigate which aspects of the pain experience are associated with burdensomeness and hopelessness at follow-up.
This study has the potential to improve the care of young people with chronic pain, and in particular the emotional support that young people receive.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Part 1: Adolescents
Part 2: Adults
Additional criteria for Part 3: Follow-up part
· In possession of a smartphone to complete the momentary assessments.
Exclusion criteria
Part 1: Adolescents
Part 2: Adults
-If the clinical care team thinks the parent/ caregiver is unsuitable for this study.
Additional criteria for Part 3: Follow-up part
-Inability to provide data via the use of a smartphone
Time frame: at baseline
Interpersonal Needs Questionnaire (INQ), completed by the adolescents. Scores range from 1="not at all true for me" to 7="very true for me", with higher scores indicating more perceived burdensomeness.
Time frame: at 7-day follow-up
Interpersonal Needs Questionnaire (INQ), completed by the adolescents. Scores range from 1="not at all true for me" to 7="very true for me", with higher scores indicating more perceived burdensomeness.
Time frame: at baseline
Hopelessness Scale for Children (HSC), completed by the adolescents. Participants score each item as 1=True and 0=False. The higher the score, the greater the hopelessness for the future.
Time frame: at 7-day follow-up
Hopelessness Scale for Children (HSC), completed by the adolescents. Participants score each item as 1=True and 0=False. The higher the score, the greater the hopelessness for the future.
Time frame: at baseline
4 single items on the presence/ absence of self-harm thoughts and acts, completed by the adolescents.
University of Oxford
Other
Exploring the Relationship Between Physical Pain and Emotional Distress in Adolescents with Chronic Pain - a Three-step Observational Follow-up Study
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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