Feasibility randomised pilot trial of Havening by zoom
- Conditions
- Post Traumatic Stress DisorderDepressionMental Health - AnxietyMental Health - DepressionAnxiety
- Registration Number
- ACTRN12621001510831
- Lead Sponsor
- Josephine Stanton
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 80
Pre recruitment adaption:
1. Aged 18 years - 75 years.
2. Having a well recalled memory of a previous event which causes them distress or symptoms.
1.People with scores above 20 on the PHQ or suicidal with plans.
2.People who are not agreeing to identify a support person and GP and give consent for them to be contacted in the context of concern about their wellbeing being identified in the course of the study.
3.People who are unable to comprehend the information sheet and the consent form.
4.People who are not fluent in English
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Between group comparison of IES scores at two-weeks and six-weeks post-intervention[IES will be measured at initial consent and screening and two and six weeks after the intervention.];Between group comparison of proportion of participants with a IES score lesser than or equal to 34 at two-weeks and six-weeks post-intervention[These scales will be measured at the time of recruitment and two and six weeks after the intervention];Qualitative information about the acceptability and feasibility of Havening via zoom. Likert scales collected at 1 and 6 week post-intervention, and two semi-structured qualitative interviews. First conducted within the first week post- intervention, and the second interview conducted at week 6. [Week 1, and week 6 post intervention]
- Secondary Outcome Measures
Name Time Method