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Psychological Benefits of Camping in Treating Children With Cancer
This study is currently recruiting participants.
Study NCT00018915   Information provided by National Cancer Institute (NCI)
First Received: July 11, 2001   Last Updated: August 19, 2009   History of Changes

July 11, 2001
August 19, 2009
March 1983
 
 
 
Complete list of historical versions of study NCT00018915 on ClinicalTrials.gov Archive Site
 
 
 
Psychological Benefits of Camping in Treating Children With Cancer
Psychological Benefits of a "Normalized" Camping Experience for Children With Cancer

RATIONALE: Children with cancer who go camping with other patients may have improved quality of life, self-esteem, and relationships with parents, family, and peers.

PURPOSE: Clinical trial to study the psychological benefits of a 1-week camping trip for children with cancer.

OBJECTIVES:

  • Determine whether quality of life, particularly sense of well being, self-esteem, and relationships with parents, family, and peers, improves in children with cancer who participate in an enriched, normalized camping experience.
  • Determine whether professional or volunteer caregivers improve the quality of their interrelations with this patient population after participating in an enriched, normalized camping experience.

OUTLINE: Patients participate in a full range of age appropriate activities and undergo observation during an enriched, normalized camping experience for 1 week. Patients and their family members undergo psychosocial interviews and patients complete psychological questionnaires before, during, and after the camping experience. Medical care continues to be provided according to the plan formulated between the patient's home medical team and the NIH-based medical team.

Quality of life is assessed.

PROJECTED ACCRUAL: Approximately 9,999 patients will be accrued for this study.

 
Interventional
Other
  • Psychosocial Effects of Cancer and Its Treatment
  • Unspecified Childhood Solid Tumor, Protocol Specific
  • Procedure: psychosocial assessment and care
  • Procedure: quality-of-life assessment
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
9999
 
 

DISEASE CHARACTERISTICS:

  • Diagnosis of cancer

    • Currently receiving treatment OR
    • No more than 3 years since prior treatment OR
  • Young adults with cancer acting as camp counselors

PATIENT CHARACTERISTICS:

Age:

  • 7 to 17

Performance status:

  • Not specified

Life expectancy:

  • Not specified

Hematopoietic:

  • Not specified

Hepatic:

  • Not specified

Renal:

  • Not specified

Other:

  • Concurrent physical defects allowed

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • Concurrent blood products allowed

Chemotherapy:

  • Not specified

Endocrine therapy:

  • Not specified

Radiotherapy:

  • Not specified

Surgery:

  • Prior amputations allowed

Other:

  • Concurrent intramuscular, intrathecal, oral, or IV medications allowed
Both
7 Years to 17 Years
No
 
United States
 
NCT00018915
 
CDR0000074606, NCI-83-C-0022F, NCI-T83-1094N
National Cancer Institute (NCI)
 
Study Chair: Stephen J. Chanock, MD National Cancer Institute (NCI)
National Cancer Institute (NCI)
November 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP