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Mental Health Wellness 1HerWellNHSNCT05701033

Does Engagement with Heritage Sites Have the Potential to Improve Sub-clinical Levels of Low Wellbeing in NHS Staff: a Feasibility Study. the HerWellNHS Study

An observational study of Mental Health Wellness 1, run by Portsmouth Hospitals NHS Trust at 1 site in United Kingdom.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This feasibility study will focus on assessing and identifying the wellbeing effects of self-directed (unmediated) visits to heritage sites for a high-risk population, specifically NHS staff at PHU self-reporting sub-clinical levels of low wellbeing. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Mental Health Wellness 1
What is being tested?
Access to heritage
How many people
250 participants
Where
1 siteUnited Kingdom
Study dates
6 Mar 2023to 3 Jan 2024
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Portsmouth Hospitals University NHS Trust staff with self-reported sub-optimal levels of wellbeing

Who may be able to join

  • The participant must meet ALL of the following criteria to be considered eligible for the study:
  • Male or Female, aged 18 years or above.
  • Self-reported subclinical levels of low wellbeing
  • Participant is willing and able to give informed consent for participation in the study.
  • NHS Staff at Portsmouth Hospitals University NHS Trust

Who cannot join

  • The participant may not enter the study if ANY of the following apply:
  • Having been diagnosed with and/or received treatment for any mental health issues in the past 12 months
  • Under 18
  • Unable to give informed consent for participation in the study

Trial locations and contacts

1 site in 1 country.

United Kingdom1 site
  • Portsmouth Hospitals University NHS Trust

    Portsmouth, Hampshire, PO6 3LY

Other trials in United Kingdom

About this study

This feasibility study will focus on assessing and identifying the wellbeing effects of self-directed (unmediated) visits to heritage sites for a high-risk population, specifically NHS staff at PHU self-reporting sub-clinical levels of low wellbeing. In particular, it seeks to understand whether wellbeing effects can be derived from unmediated visits to heritage sites, how much exposure to heritage is necessary to experience wellbeing effects, whether and how benefits may be accumulated, how long wellbeing effects may last following visits, and the nature of these wellbeing effects. In addition, it will establish appropriate psychological measures (qualitative and quantitative), test a web-based data collection interface, examine participant choices and their characteristics, and assess participant adherence and response rates prior to developing a clinical trial.

Read the detailed description

This feasibility study will use quantitative and qualitative psychological measures to examine participant choices of heritage sites and their characteristics, as well as assessing participant adherence and response rates prior to development of a future clinical trial.

It will act as proof of concept, generating a case for the promise of unmediated heritage visits as an effective mental health intervention.

The project will focus on assessing and identifying the wellbeing effects of unmediated visits to heritage sites for NHS staff, and seeks to understand how much exposure to heritage is necessary to experience wellbeing effects, how benefits may be accumulated, how long wellbeing effects may last following a visit, and what the nature of these wellbeing effects may be. The study also seeks to capture the staff experience of engaging with heritage sites, what are the aspects which might result in positive change as a result of the interactions as well if there are any potential risks associated with such interventions.

This project is funded by Historic England. The project partners are as follows: Portsmouth University NHS Hospitals, The Royal Navy National Museum, The Mary Rose Museum, Wessex Archaeology, Portsmouth City Council, Art as Media and the University of Southampton.

Being tested
Access to heritage

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Access to heritageOther

    Unmediated access to heritage sites for wellbeing

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. improve sub-clinical levels of low wellbeing for staff

    As a primary objective, this feasibility study aims to determine whether engagement with heritage sites has the potential to improve sub-clinical levels of low wellbeing for staff at Portsmouth Hospitals University NHS Trust.

    Measured: Through study completion, an average of 6 months

Secondary outcomes (5)
  1. What intensity of exposure to heritage is necessary to experience wellbeing effects, and whether and how benefits may be accumulated?

    What intensity of exposure to heritage is necessary to experience wellbeing effects, and whether and how benefits may be accumulated?

    Measured: Through study completion, an average of 6 months

  2. What kinds of wellbeing benefits do staff experience?

    What kinds of wellbeing benefits do staff experience?

    Measured: Through study completion, an average of 6 months

  3. What other 'spin-off' effects might be obtained through improved staff wellbeing via visits to heritage sites?

    What other 'spin-off' effects might be obtained through improved staff wellbeing via visits to heritage sites?

    Measured: Through study completion, an average of 6 months

  4. What factors are related to the wellbeing effects of heritage visits (e.g. exercise, being with other people, duration of visit, type of heritage visit)?

    What factors are related to the wellbeing effects of heritage visits (e.g. exercise, being with other people, duration of visit, type of heritage visit)?

    Measured: Through study completion, an average of 6 months

  5. What is the duration of post-visits effectiveness on wellbeing?

    What is the duration of post-visits effectiveness on wellbeing?

    Measured: Through study completion, an average of 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Jan 2023
  2. Study start6 Mar 2023
  3. Primary completion3 May 2023
  4. Study completion3 Jan 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Prospective
Enrolment
250 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05701033
Sponsor's protocol ID
PHU/2022/68
Acronym
HerWellNHS
Status last verified
Nov 2024
First submitted
13 Dec 2022
Last updated
7 Nov 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Data to be pseudo anonymised where possible and only available to thre research team

Questions about this trial

What is this clinical trial studying?

An observational study of Mental Health Wellness 1, run by Portsmouth Hospitals NHS Trust at 1 site in United Kingdom.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 7 Nov 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

improve sub-clinical levels of low wellbeing for staff (time frame: Through study completion, an average of 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Nov 2024.

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