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Resiliency Training for Patients With NF2 Via Videoconferencing With Skype

Mass General Brigham logo

Mass General Brigham

Status

Completed

Conditions

Neurofibromatosis 2

Treatments

Behavioral: Stress Management Group 1
Behavioral: Stress Management Group 2

Study type

Interventional

Funder types

Other

Identifiers

NCT02811718
2013P002605b

Details and patient eligibility

About

The aim of this study is to determine, whether the 3RP is feasible, accepted and efficacious and durable when delivered via Skype to patients with neurofibromatosis type 2 (NF2) who are deaf or have severe hearing loss using Communication Access Realtime Translation (CART) and/or American Sign Language (ASL).

This will be a substudy of the IRB-approved protocol #2013P002605. It is the same study except it is looking at a particular sub-population: patients with NF2 who are hard of hearing.

Enrollment

45 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age 18 or older
  2. Can read and speak English at or above the 6th grade level
  3. Patients with NF2 who are deaf or have severe hearing loss.

Exclusion criteria

  1. Severe active or untreated major mental illness that would interfere with study participation, to be determined at the discretion of the study investigator (e.g. untreated psychosis or suicidality)
  2. Recent (within past 3 months) change in antidepressant medication
  3. Use of formal relaxation training (including past participation in a mind-body program), currently or in the past 6 months.
  4. Unable or unwilling to sign the informed consent documents
  5. Unable or unwilling to complete psychological assessments online via the REDCap system.
  6. Unable or unwilling to participate in an intervention delivered via videoconferencing with Skype.
  7. Unwilling to use either CART or ASL for communication during the Skype groups.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

45 participants in 2 patient groups

Stress Management Group 1
Experimental group
Description:
Subjects will attend group stress management sessions via Skype once weekly for 8 weeks and learn stress/NF symptoms managements techniques.
Treatment:
Behavioral: Stress Management Group 1
Stress Management Group 2
Experimental group
Description:
Subjects will attend group stress management sessions via Skype once weekly for 8 weeks and learn stress/NF symptoms managements techniques.
Treatment:
Behavioral: Stress Management Group 2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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