NCT01182857

Quality of Life and Neuropsychiatric Sequelae in Patients Treated With Gene Therapy for ADA-SCID and in Their Parents

Withdrawn Last updated 17 December 2019

What this trial tests

trial in ADA-SCID. Withdrawn.

Timeline

5 August 2010

25 September 2014

Quick facts

Lead sponsor	National Human Genome Research Institute (NHGRI)
Status	Withdrawn
Study type	OBSERVATIONAL
Start date	5 August 2010
Estimated completion	25 September 2014

Conditions studied

• ADA-SCID — all drugs for ADA-SCID →

Sponsor

National Human Genome Research Institute (NHGRI)

Who can join

Adults 5 Months to 50, any sex, with ADA-SCID. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Background:

* Severe combined immunodeficiency (SCID) is a rare inherited disorder in which certain white blood cells have impaired function and are unable to properly fight infections. SCID typically appears within the first year of life and is characterized by multiple, recurrent severe infections. More than 10 percent of all cases of SCID involve a deficiency of an enzyme called adenosine deaminase (ADA), and these SCID patients also tend to have impaired brain function or psychiatric disorders. Researchers are attempting to treat ADA-SCID patients with an experimental gene therapy, and a research protocol has been established for those who are participating in this therapy.
* Little is known about quality of life in individuals with ADA-SCID, but researchers believe that the effects of the disease and the treatments may cause a decreased quality of life in both patients and their parents. Another potential cause of decreased quality of life in ADA-SCID is the associated psychiatric and neurological problems caused by the disease. Researchers are interested in studying quality of life in individuals with ADA-SCID and their parents to provide more information about the disease.

Objectives:

* To evaluate whether gene therapy alters the quality of life or neuropsychiatric status of children with ADA-SCID.
* To monitor for intellectual, attention, memory, or specific learning disorders in children with ADA-SCID.
* To evaluate whether undergoing gene therapy has an effect on parenting stress of parents whose children have ADA-SCID.

Eligibility:

* Children who are participating in the ADA-SCID gene therapy research protocol (01-HG-0189).
* Parents of children who are participating in the ADA-SCID gene therapy research protocol (01-HG-0189).

Design:

* All of the testing and questionnaires will be done in the pediatric or adult clinic.
* Participating children will have tests of intelligence, manual dexterity, reaction time, basic reading and arithmetic skills, speech, and memory. These tests will be given before the start of the therapy, and then once a year for 5 years.
* Participating children will also complete questionnaires on quality of life. These questionnaires will be given before the start of the therapy, 3 months and 6 months after the therapy, and then every 6 months for a total of 5 years.
* Additional psychological tests may be given at the discretion of the study researchers.
* Parents will complete questionnaires to provide background medical information and report on quality of life and parental stress. The background information questionnaires will be given at the start of the therapy and then once a year for 5 years, the parental stress questionnaires will be given at the start of the therapy and then every 6 months for 5 years, and the quality of life questionnaires will be given at the same time as the child quality of life questionnaires.
* This protocol is separate from the gene therapy treatment protocol.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.