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OpenTrials
Completed

NCT Number: NCT00086021

Acupuncture for the Treatment of Chronic Daily Headaches

The purpose of this study is to determine whether acupuncture can reduce pain in long-term headache sufferers.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Harvard Medical School, Boston, Massachusetts, United States

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About this study

Acupuncture has been shown to reduce the frequency and severity of some types of headaches, but the efficacy of acupuncture for chronic daily headaches has not been studied. The long-term goals of this study are to reduce the symptoms that are associated with recurrent headaches and to collect data that can be used for future acupuncture studies.

Participants in this study will be randomly assigned to receive 8 weeks of either standard care or ten acupuncture treatments in addition to medical care. Self-report questionnaires will be used to assess headaches and daily pain severity.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Ability to communicate in English
  • Presence of headache 15 or more days in the past month

Exclusion criteria

  • Known intracranial mass
  • Recent surgery to the head and neck region

Treatment and study plan

Acupuncture

Procedure

Sponsors and collaborators

Lead sponsor

National Center for Complementary and Integrative Health (NCCIH)

Nih

Registry information

Important dates

Study start
2002
Study completion
2007
First posted
Jun 22, 2004
Registry last updated
Jun 11, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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