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OpenTrials
Completed

NCT Number: NCT02195674

EMBARK Follow-up Project

The purpose of the EMBARK Follow-up Project (EFP) is to determine if there is a significant correlation between post-study massage-seeking and changes in pain reported by participants during the Exploring Massage Benefits for Osteoarthritis of the Knee (EMBARK) parent study (NCT00970008). The EFP hypothesizes that a positive correlation exists between pain relief during the parent study and post-study massage-seeking behavior.

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Key information

Age range

35 year and older

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Completed in the EMBARK parent study.

Exclusion criteria

  • Did not complete the EMBARK parent study.

Treatment and study plan

Primary outcomes

  1. EMBARK Follow-up Project Questionnaire (EFPQ)

    Time frame: Eight weeks

    The EFPQ is an original set of questions, designed and validated by Dr. Jerger under the supervision of NCCAM and Dr. Ruth Wolever to be administered by email or phone to address the specific aims of this project.

Sponsors and collaborators

Lead sponsor

Duke University

Other

Collaborators

  • National Center for Complementary and Integrative Health (NCCIH)

Registry information

Official study title

Exploring Massage Benefits for Arthritis of the Knee (EMBARK): Post-study Massage Questionnaire

Acronym: EFP

Important dates

Study start
2013
Primary completion
2015
Study completion
2015
First posted
Jul 21, 2014
Registry last updated
Nov 16, 2015

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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