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Intervention for Sleep and Pain in Youth

Not Applicable
Completed
Conditions
Migraine Disorders
Insomnia
Headache Disorders
Interventions
Behavioral: Intervention for Sleep and Pain in Youth
Registration Number
NCT03137147
Lead Sponsor
Seattle Children's Hospital
Brief Summary

This study tests the feasibility, acceptability, and preliminary efficacy of a seven-session cognitive-behavioral therapy intervention to treat sleep and pain problems in youth ages 11-17 with co-morbid headache and insomnia.

Detailed Description

Cognitive-behavioral interventions have been developed to treat childhood insomnia and childhood headache. In this study, we have combined strategies from these interventions into a single, seven-session protocol to treat sleep and pain problems in youth with co-morbid headache and insomnia. In this single-arm pilot study, we will test the feasibility, acceptability, and preliminary efficacy of this intervention.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
21
Inclusion Criteria
  • youth age 11-17 years
  • chronic headache and insomnia symptoms for the past 3 months as determined on screening interview with youth and parent.
Exclusion Criteria
  • youth and parent do not read or speak English
  • youth with active suicidal ideation or psychosis
  • youth with diagnosis of a comorbid serious health condition (e.g., cancer, diabetes)
  • youth with severe cognitive impairment
  • youth with another primary sleep disorder (e.g., sleep apnea, narcolepsy) or an unusual sleep/wake schedule or circadian rhythm disorder.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Cognitive-Behavioral TherapyIntervention for Sleep and Pain in YouthIntervention for Sleep and Pain in Youth, a 7-session cognitive-behavioral therapy intervention for co-morbid insomnia and headache
Primary Outcome Measures
NameTimeMethod
Feasibility of Intervention Delivery: Number of Completed Intervention Visits6-12 weeks

Number of completed intervention visits

Feasibility of Intervention Delivery: Recruitment/Enrollment Rate6-12 weeks

Recruitment/Enrollment Rate

Secondary Outcome Measures
NameTimeMethod
Treatment Acceptability and Satisfaction: Treatment Evaluation Inventory Short Form3 months

9-item self-report measure of treatment acceptability and satisfaction, scores range from 9-45, higher scores indicate greater treatment acceptability

Insomnia Severity Index3 months

7-item self-report measure of insomnia severity and impact, scores range from 0-28 with higher scores indicating greater insomnia symptoms.

Adolescent Sleep Wake ScalePast 4 weeks

28-item measure of subjective sleep quality, scores range from 28-168, higher scores indicate poorer sleep quality

Pain QuestionnairePast 2 weeks

Assesses pain frequency, intensity, onset, and duration.

Child Activity Limitations InterviewPast month

Assesses pain-related disability

Trial Locations

Locations (1)

Seattle Children's Research Institute

🇺🇸

Seattle, Washington, United States

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