Cygnet Maidstone Hospital
Maidstone, Kent, ME14 5FY, United Kingdom
NCT Number: NCT06905184
Design
A quasi-experimental mixed methods design research study will be conducted within:
Pippin Ward, a 10 bed Female PICU within Cygnet Appletree (data collected January - June 2022).
Haywood Ward, a 16 Male Acute within Cygnet Kewstoke. Nash Ward, a 12 bed Male PICU within Cygnet Kewstoke. Sandford Ward, a 16 bed Female Acute within Cygnet Kewstoke. Juniper Ward, a 17 bed Male Acute within Cygnet Churchill. Castle Ward, a 12 bed Female PICU within Cygnet Godden Green. Oakwood ward, a 15 bed Female Acute within Cygnet Godden Green.
The study will measure the change in provision of meaningful activity types, and frequency of participation within meaningful activities, as a result of the intervention, 'Activity PRN', on participating wards within Cygnet Healthcare Ltd.
Activity PRN, is an approach that uses occupational therapy approaches to facilitate meaningful activities as and when required. A 'prn activity' is any personally meaningful activity which can be facilitated as and when required, and is not a timetabled activity or session.
To show the effect of the intervention, a three month control period, pre-intervention, will measure the number of meaningful activity types provided, facilitated on an 'ad-hoc' basis, and participation frequency. A two week period will follow, in which ward based staff will receive training to implement Activity PRN. A further three month intervention period will measure the number of prn activity types provided, and the participation frequency of prn activities, as a result of delivering Activity PRN. It is hoped that about 60 patients will consent to receive the intervention.
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Notify Me18 year–65 year
All sexes
Interventional
Not applicable
Maidstone, Kent, ME14 5FY, United Kingdom
Ethical considerations All patients are invited to take part in the study, unless for any reason the Multi-Disciplinary Team decides that the patient is unsafe to take part, or cannot otherwise engage in meaningful activities on an as and when required basis.
Patients are selected to take part in the study by decision of their Multi-Disciplinary Team, that they have the capacity to make the decision to take part. At this point they are invited to read a Participant Information Sheet (appendix one), and given the opportunity to ask questions and clarify understanding of what the study involves and what they will need to do.
Patients are then asked to sign an Informed Consent Form (appendix two), to confirm understanding and that they agree to take part. A witness will also sign the form, who will be the occupational therapist or occupational therapy assistant on the ward. They have a right to withdraw their consent without affecting their rights as a patient.
After the informed consent form is signed, the patient is asked to contact their occupational therapist or occupational therapy assistant to start receiving the intervention, and a contact telephone and email for them is given on the patient information sheet.
Activity PRN is still offered as an intervention even if the patient declines to take part in the study.
Pre-Intervention To deliver the control intervention, Activity PRN is not implemented during an initial three month period. Patients however will have access to ad-hoc personally meaningful activities as part of a general ward environment. To maintain effect of the control period, neither ward staff nor patients will be made aware of the study.
To measure the number of ad-hoc meaningful activity types provided, and participation frequency, the following will be carried out:
Staff Training
A two-week break will take place following the pre-intervention to deliver staff training. As part of the training course, the following will take place:
The project manager facilitates training sessions using virtual technology, and where possible in house training until the whole ward team is trained. Nursing and support staff are supported to learn Activity PRN terminology, use the activity cards and engage service users in their prn activities, and record activity participation.
Intervention
To deliver Activity PRN as an intervention over a three month period, the following will be carried out:
To measure the number of prn activity types provided, and participation frequency, the following will be carried out:
Data Processing
To process results, the following will be carried out:
Study Limitations
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Male or Female 18-65 Any ethnicity Any socio economic grouping Must be admitted to hospital for any primary diagnosis of a mental health condition Location as per units referred to in the study setting
Exclusion criteria
Excluded participants are those who do not give informed consent, or cannot give informed consent by review of the Multi-Disciplinary Team within participating wards.
An Activity PRN plan will be delivered to consenting patients, as described above. The intervention will be communicated to them as a new approach that 'supports the individual to engage in personalised meaningful activities, which they can engage in as and when required'.
Activity Resources are organised within a suitable, accessible location according with the patient's risk management and support plan. Dependent on the plan, resources may be kept on their person, in their bedroom, in a communal area, or in a locked or unlocked accessible cupboard.
Ward staff will facilitate prn activities on an 'as and when required' basis. This can occur when: 1) a patient requests an activity from their card, 2) the patient appears disengaged, or 3) staff deem that the patient may benefit from participation in an activity for the purpose of engagement or distraction.
Time frame: 6 months
An increase in provision of 'as when required' (prn) activities across all services monitored.
Time frame: 6 months
An increase in participation frequency of 'prn activities', compared to 'ad hoc' meaningful activities pre-intervention.
Cygnet Healthcare
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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