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N/A Completed N=38 Supportive Care

Culturally Adapted Mobile Treatment of Chronic Pain in Adolescent Survivors of Pediatric Cancer

Bone Sarcoma · Childhood Cancer
Source: ClinicalTrials.gov NCT05746429 ↗
Enrolled (actual)
38
Serious AEs
0.0%
Results posted
Feb 2026
Primary outcomePrimary: Pain Intensity — -0.96; -0.56 Change in scores on a scale

Summary

This is a prospective study that will conduct a series of focus groups with non-Hispanic Black and Hispanic childhood cancer survivors to obtain their input on culturally adapting a mobile CBT program for chronic pain and tDCS procedures. Once this adaptation process is completed, the investigators will conduct a feasibility trial with non-Hispanic Black, Hispanic and non-Hispanic White survivors of childhood cancer with chronic pain. The feasibility study will assign eligible participants to either culturally adapted mobile CBT + active tDCS to the dorsolateral prefrontal cortex or culturally adapted mobile CBT + sham tDCS. We anticipate approximately 60 participants for the focus groups and approximately 30 participants for the feasibility study for a total of about 90 participants.

Outcome Measures

OutcomeResultp-value
PRIMARY
Pain Intensity
-0.96; -0.56
PRIMARY
Pain Interference
-0.60; -1.30
PRIMARY
Pain Catastrophizing
-0.07; -1.13; -0.64; -0.69; 1.07; -1.81
PRIMARY
Depression
-0.65; -3.13
PRIMARY
Anxiety
-3.82; -2.01
PRIMARY
Cancer-related Worry
3.64; -4.13
PRIMARY
Physical Functioning
0.34; 4.03; 1.94; 0.42
PRIMARY
Peer Relations
-1.64; -3.26
PRIMARY
Fatigue
-2.72; -2.86
PRIMARY
Sleep (Adolescent Sleep Wake Scale (ASWS))
-0.20; 0.61
PRIMARY
Sleep (PROMIS Sleep-related Impairment)
-0.51; -2.76
PRIMARY
Global Acceptability and Satisfaction With Treatment
3; 10; 11; 6; 8; 12
PRIMARY
Opioid Use
0; 0
PRIMARY
Parental Depression
-2.00; -1.19
PRIMARY
Parental Anxiety
-0.93; -1.14

Eligibility Criteria

Inclusions Criteria for cultural adaption

  • Adult
  • Hispanic or non-Hispanic Black childhood cancer survivor or parent of Hispanic or non-Hispanic Black childhood cancer survivor
  • 18 years or older
  • Adolescents
  • 10-17 years-old survivors of childhood cancer
  • At least one year post treatment
  • Hispanic or non-Hispanic Black
  • Phase 4 only: History of chronic pain (i.e. pain that was present for more than 3 months)

Exclusion Criteria for cultural adaptation

  • Adults/Adolescents
  • Inability or unwillingness of research participants or legal guardian/representative to give written informed consent

Inclusion Criteria for feasibility study

  • Hispanic, non-Hispanic Black and non-Hispanic White 10-17-year-old survivors of pediatric cancer
  • At least one year post treatment
  • Pain present over the past 3 months and pain at least once per week
  • Pain interfering with at least one area of daily functioning

Exclusion Criteria for feasibility study

  • Limb amputation
  • History of seizures or other neurological disorders
  • Implanted medical device or metal in the head
  • Serious comorbid psychiatric condition
  • Current substance abuse
  • History of development delay or significant cognitive impairment
  • History of brain tumor diagnosis
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05746429). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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