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Clinical Trial Summary

The purpose of this study is to compare reflexology to meditative practices to reduce symptoms in cancer patients.


Clinical Trial Description

First, dyads were randomized to receive caregiver-delivered reflexology or meditative practice. Fatigue severity was assesses weekly via phone calls to the cancer patients during weeks 1-4 of the intervention. For patients who did not respond to the intervention during the first 4 weeks, those dyads were referred to as non-responder and re-randomized. A non-responder was determined if the level of reported fatigue remained the same or increased from the first week of the intervention. The re-randomization placed the non-responders in either a group that received a higher dose (more time) with the first intervention or to the alternate practice (meditative practice to those randomized to reflexology and vice versa) for weeks 5-8. Those who did respond during weeks 1-4 continued the same therapy they began with. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02759146
Study type Interventional
Source Michigan State University
Contact
Status Completed
Phase N/A
Start date May 2016
Completion date November 2019

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