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Therapeutic Touch for Wrist Fractures in Postmenopausal Women - Article


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Fractures

Broken Bones; Fracture 




Clinical Trial: Therapeutic Touch for Wrist Fractures in Postmenopausal Women

This study is currently recruiting patients.

Sponsored by: National Center for Complementary and Alternative Medicine (NCCAM)
Information provided by: National Center for Complementary and Alternative Medicine (NCCAM)

Purpose

This study will evaluate the effectiveness of therapeutic touch in treating wrist fractures in women past menopause.

Condition Treatment or Intervention Phase
Osteoporosis
Fractures
 Procedure: Therapeutic Touch
Phase II

MedlinePlus related topics:  Fractures;   Osteoporosis

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Factorial Assignment, Efficacy Study

Official Title: The Effect of Therapeutic Touch on Bone Formation in Postmenopausal Women After Wrist Fracture

Further Study Details: 

Expected Total Enrollment:  125

Study start: March 2003

In the United States, the use of complementary and alternative medicine (CAM) increased by approximately 25% between 1990 and 1997. The number of visits to CAM practitioners exceeded visits to primary care physicians by about 250 million in 1997. Energy medicine modalities, including therapeutic touch, healing touch, and reiki, are commonly utilized for conditions ranging from headache to cancer, yet understanding of the human energy field and how it may be used in healing is limited. This study will examine the effect of therapeutic touch on fracture healing in postmenopausal women.

Women will be enrolled in the study within one week of a wrist fracture and will receive either therapeutic touch or a sham (placebo) treatment daily for 3 weeks. Assessments will include blood and urine analysis and measures of pain and function in the affected wrist.

Eligibility

Ages Eligible for Study:  40 Years   -   85 Years,  Genders Eligible for Study:  Female

Accepts Healthy Volunteers

Criteria

Inclusion Criertia:

  • Postmenopausal
  • Wrist fracture within 1 week of study entry
  • Able to travel to research center for daily treatment

Location and Contact Information


Connecticut
      University of Connecticut Health Center, Farmington,  Connecticut,  06030-5215,  United States; Recruiting
Karen M Prestwood, MD  860-679-4549    prestwood@uchc.edu 
Thomas Shepherd, BA  860-679-4994    shepherd@nso1.uchc.edu 
Karen M Prestwood, MD,  Principal Investigator
Mary Lynn Newport, MD,  Sub-Investigator
Anne M Kenny, MD,  Sub-Investigator

Study chairs or principal investigators

Karen M. Prestwood, MD,  Principal Investigator,  University of Connecticut   

More Information

Study ID Numbers:  1 P20 AT00756-01P1
Record last reviewed:  April 2005
Last Updated:  April 7, 2005
Record first received:  March 9, 2004
ClinicalTrials.gov Identifier:  NCT00079521
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005

Resources



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Page Updated: December 9, 2005
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