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Completed

NCT Number: NCT03873610

Resiliency Training in Adolescents With NF1 and NF2

This randomized controlled trial for resiliency training in adolescents with Neurofibromatosis 1 and Neurofibromatosis 2 via secure live video to determine the efficacy two stress and symptom management programs. Both programs are 8 week group programs.

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Key information

About this study

Neurofibromatosis (NFs) are rare genetic conditions with cure. Adolescents with NF experience more symptoms of depression and anxiety, higher levels of stress associated with coping with NF symptoms, lower levels of self esteem, difficulties with social skills and social support, high rates of learning disabilities, and more pain as compared with the general population norms.

The aims of this study are to compare the effect of two stress and symptom management programs tailored for adolescents with neurofibromatosis on quality of life and psychosocial functioning. We will also examine the degree to which treatment-dependent improvements in quality of life are mediated by improvements in depression, pain intensity and pain interference.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Has a diagnosis of NF1 or NF2 and is between the ages of 12-17
  • Is capable of completing and fully understanding the informed consent process/assent and the study procedures and assessments in English; has parental approval for participation
  • English speaking and at least a 3rd grade self-reported and parent reported reading level
  • Self reported/parent reported difficulties coping with stress and NF symptoms

Exclusion criteria

  • Has major medical co-morbidity not NF related expected to worsen in the next 12 months
  • Recent (within past 3 months) change in antidepressant medication
  • Recent participation in cognitive behavioral therapy or relaxation therapy (within past 3 months)
  • Has significant mental health diagnosis requiring immediate treatment (e.g., untreated bipolar disorder, psychotic disorder, active substance dependence)
  • Unable or unwilling to complete assessments electronically via REDCap
  • Unable or unwilling to participate in group videoconferencing sessions
  • Unable or unwilling to participate along with at least 1 parent in a video screening session

Treatment and study plan

Stress and Symptom Management Program 1

Behavioral

The Stress and Symptom Management Program 1 introduces and reinforces stress and symptom management for adolescents with NF. The program consists of 8 weekly 45 minute sessions, delivered through videoconferencing.

Stress and Symptom Management Program 2

Behavioral

The Stress and Symptom Management Program 2 introduces and reinforces stress and symptom management for adolescents with NF. The program consists of 8 weekly 45 minute sessions, delivered through videoconferencing.

Primary outcomes

  1. Change in Physical Health Quality of Life

    Time frame: 0 weeks, 8 weeks, 6 months,12 months

    World Health Organization Quality of Life Brief (WHOQOL-BREF); 4-20; Higher score indicates higher QoL

  2. Change in Psychological Health Quality of Life

    Time frame: 0 weeks, 8 weeks, 6 months,12 months

    World Health Organization Quality of Life Brief (WHOQOL-BREF); 4-20; Higher score indicates higher QoL

Secondary outcomes

  1. Social relationships Quality of Life

    Time frame: 0 weeks, 8 weeks, 6 months,12 months

    World Health Organization Quality of Life Brief (WHOQOL-BREF); 4-20; Higher score indicates higher QoL

  2. Environmental Quality of Life

    Time frame: 0 weeks, 8 weeks, 6 months, 12 months

    World Health Organization Quality of Life Brief (WHOQOL-BREF); 4-20; Higher score indicates higher QoL

  3. Depression

    Time frame: 0 weeks, 8 weeks, 6 months, 12 months

    Patient Health Questionnaire (PHQ-9) Adolescent Version; 0-27; Higher score indicates more symptoms of depression

  4. Anxiety

    Time frame: 0 weeks, 8 weeks, 6 months, 12 months

    Generalized Anxiety Disorder (GAD-7) Questionnaire; 0-21; Higher score indicates more symptoms of anxiety

  5. Pain intensity

    Time frame: 0 weeks, 8 weeks, 6 months, 12 months

    Numerical Rating Scale; 0-10; Higher score indicates more intense pain.

  6. Pain interference

    Time frame: 0 weeks, 8 weeks, 6 months, 12 months

    Pain Interference Index (PII); 0-36; Higher score indicates more pain interference

Sponsors and collaborators

Lead sponsor

Massachusetts General Hospital

Other

Collaborators

  • United States Department of Defense

Registry information

Official study title

Resiliency Training in Adolescents With NF1 and NF2; A Randomized Controlled Trial Via Secure Live Video Conferencing to Improve Emotional, Social and Physical Function

Important dates

Study start
2019
Primary completion
2026
Study completion
2026
First posted
Mar 13, 2019
Registry last updated
Jun 11, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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