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NCT05746429Completed

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

Culturally Adapted Mobile Treatment of Chronic Pain in Adolescent Survivors of Pediatric Bone Sarcoma

Source: ClinicalTrials.gov · Last updated 4 Feb 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
68 (actual)
First submitted
10 Jan 2023
Start date
Apr 2023
Primary completion date
Oct 2024
Lead sponsor
St. Jude Children's Research Hospital
NCT number
NCT05746429

What you commit to

  • Study type: Interventional
  • Participants enrolled: 68
  • From Apr 2023 to the primary completion date, Oct 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • History of seizures or other neurological disorders
  • Serious comorbid psychiatric condition
  • History of development delay or significant cognitive impairment
  • History of brain tumor diagnosis

Other

  • Adults/Adolescents
  • Inability or unwillingness of research participants or legal guardian/representative to give written informed consent
  • Limb amputation
  • Implanted medical device or metal in the head
  • Current substance abuse

Who the study is looking for

  • 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

Criteria the registry did not label

  • 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)

Age in the registry: 10 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
St. Jude Children's Research Hospital
Coordinator of this site? Confirm its status
MemphisUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.