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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Psychosensory Therapy | Havening 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.