Clinical Trials Directory

Trials / Completed

CompletedNCT03568591

The Efficacy of a Psychosomatic Intervention

A Parallel-Group Controlled Trial Examining the Efficacy of a Psychosomatic Intervention

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
125 (actual)
Sponsor
Cardiff Metropolitan University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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).

Detailed 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).

Conditions

Interventions

TypeNameDescription
PROCEDUREPsychosensory TherapyHavening Techniques are a psychosensory therapy that incorporate the application of sensory input to alter neurochemical responses influencing thought, emotion and behaviour (Ruden, 2011).

Timeline

Start date
2016-06-11
Primary completion
2016-10-31
Completion
2016-11-01
First posted
2018-06-26
Last updated
2018-06-26

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT03568591. Inclusion in this directory is not an endorsement.