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NCT00079521 Clinical Trial

Therapeutic Touch for Wrist Fractures in Postmenopausal Women

Osteoporosis Clinical Trial

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00079521
Other study ID # P20 AT000756-01P1
Secondary ID
Status Completed
Phase Phase 2
First received March 9, 2004
Last updated August 16, 2006
Start date March 2003
Est. completion date April 2006

Study information
Verified date August 2006
Source National Center for Complementary and Integrative Health (NCCIH)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

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

Description:

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.

Recruitment information / eligibility
Status Completed
Enrollment 125
Est. completion date April 2006
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 40 Years to 85 Years
Eligibility Inclusion Criertia:

- Postmenopausal

- Wrist fracture within 1 week of study entry

- Able to travel to research center for daily treatment

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Procedure:
• Therapeutic Touch

Locations
Country Name City State
United States University of Connecticut Health Center Farmington Connecticut

Sponsors (1)
Lead Sponsor Collaborator
National Center for Complementary and Integrative Health (NCCIH)

Country where clinical trial is conducted

United States, 

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