The Efficacy of a Psychosomatic Intervention

Status Completed

Clinical Trial Summary

This study examines the efficacy of a psychosensory intervention in relation to: Resilience, Type D personality, and physiological effects (on blood pressure, heart rate and salivary cortisol) in a group of people who have self-referred for the trauma resolution psychosensory therapy - Havening Techniques (HT).

Clinical Trial Description

This study utilizes a single blind (researcher blind) comparison of the psychosensory therapy Havening Techniques (treatment) versus waiting list (no treatment). Participants will be assessed using resilience testing (CD-RISC), and Type D measure of personality (DS14). A subgroup of the treatment arm will be assessed for the biomarkers of blood pressure, heart rate and cortisol. This parallel-group controlled trial will examine the efficacy of Havening Techniques at 3 timepoints; baseline (Time point 1), twenty-four hours post (Time point 2) and one month later (Time point 3). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03568591
Study type	Interventional
Source	Cardiff Metropolitan University
Contact
Status	Completed
Phase	N/A
Start date	June 11, 2016
Completion date	November 1, 2016

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