Resilience, PsychologicalNCT07155512
Impact of a Bespoke Mindfulness Intervention for Registered Dietitians on Resilience, Burnout and Stress
A study testing Mindfulness based intervention in people with Resilience, Psychological and Burnout, Professional, run by University of Nottingham at 1 site in United Kingdom.
Trial summary
The goal of this randomised control trial is to find out whether a mindfulness based intervention can improve mental well-being for Registered Dietitians (RD) in the UK. The main question it aims to answer is: Can a mindfulness based intervention improve resilience amongst UK RDs? Can a mindfulness based intervention… Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Resilience, Psychological, Burnout, Professional, Stress, Psychological
- What is being tested?
- Mindfulness based intervention
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 30 participants
- Where
- 1 siteUnited Kingdom
- Study dates
- 8 Mar 2024to 19 Jun 2025
- Phase
- Interventional
- 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
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- A Registered Dietitian currently practicing in the UK
- Willing and able to participate in 4 x 50 minute CPD sessions relating to mindfulness in dietetic practice (one session per week)
- Willing and able to complete all of the surveys (pre-intervention, immediately post, 3 months post and 6 months post intervention)
Who cannot join
- A diagnosis of a psychotic condition
- A diagnosis of epilepsy or asthma that is not well controlled
Trial locations and contacts
1 site in 1 country.
About this study
Official title: The Impact of a Bespoke Mindfulness Intervention for Registered Dietitians on Resilience, Burnout and Stress - A Cluster Randomised Control Trial
The goal of this randomised control trial is to find out whether a mindfulness based intervention can improve mental well-being for Registered Dietitians (RD) in the UK. The main question it aims to answer is:
Can a mindfulness based intervention improve resilience amongst UK RDs?
Read more
Can a mindfulness based intervention reduce stress and burnout amongst UK RDs?
Researchers will compare participants who attend a structured mindfulness based intervention with a waitlist control group to see if there is a difference in outcome measures between the groups before the intervention, immediately after, 3 months after and 6 months after.
Participants in the intervention group will be invited to an online mindfulness course that was written especially for this study. Participants in both groups will be asked to complete surveys before the intervention, immediately after, 3 months after and 6 months after. Participants in the intervention group will also be invited to participate in a one to one interview to discuss their experiences, barriers and facilitators to mindfulness in dietetic practice.
- Being tested
- Mindfulness based intervention
- Keywords
- Registered Dietitian, Mindfulness, Randomised control trial, Resilience, Burnout, Stress, Mindfulness based intervention, Health personnel, Continuing professional development, Occupational health
- Medical subject headings
- Burnout, Professional, Stress, Psychological, Burnout, Psychological
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Mindfulness based interventionBehavioural
A mindfulness intervention was designed especially for this study and delivered by a RD also qualified as a mindfulness teacher. The intervention was delivered synchronously online and consisted of 4 x 50 minute sessions delivered across 4 weeks.
| Study group | Role | What they receive |
|---|---|---|
| Mindfulness based intervention | Experimental | Mindfulness based intervention (delivered synchronous online) Receives: Behavioral: Mindfulness based intervention |
| Waitlist control group | No intervention | No intervention provided during the data collection period. Mindfulness based intervention delivered after data collection period. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Resilience
Measured using validated tool: Brief Resilience Scale. Scores range from 1-5. Higher scores = higher level of resilience. 1.00-2.99= Low resilience; 3.00-4.30 = Normal resilience; 4.31-5.00= High resilience.
Measured: Baseline, immediately after intervention (at the end of the last session of the 4 week intervention), 3 months post intervention, 6 months post intervention
Secondary outcomes (2)
Burnout
Measured using validated tool: Maslach Burnout Inventory, which has 3 domains which have the following scoring:
Emotional Exhaustion (EE): </=17 low/more favourable; 18-29 moderate; >/= 30 high / least favourable Depersonalisation (DP): </=5 low/ more favourable; 6-11moderate; >/=12 high / least favourable Personal Accomplishment (PA): </=33 low / least favourable; 34-39moderate; </=40 high / most favourable
Measured: Baseline, immediately post (this survey is administered at the end of the 4th and final session of the intervention, which was week 4), 3 months post, 6 months post intervention
Stress
Measured using validated tool: Perceived Stress Scale - scores range from 0-40 with higher scores indicating higher levels of perceived stress.
Measured: Baseline, immediately post intervention (this survey was given at the end of the 4th and final session of the intervention), 3 months post intervention, 6 months post intervention
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Sep 2025
- Study start8 Mar 2024
- Primary completion19 Jun 2025
- Study completion19 Jun 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Resilience, PsychologicalStudies of the same condition, open and under way.
- More trials run by University of NottinghamThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 30 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Nottingham
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07155512
- Sponsor's protocol ID
- FMHS 70-1123
- Status last verified
- Aug 2025
- First submitted
- 12 Aug 2025
- Last updated
- 4 Sep 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: Data collected in respect of 3 outcomes measured (resilience, burnout and stress) can be shared if required.
Study at a glance
From the registry record, last updated by the sponsor on 4 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Impact of a Bespoke Mindfulness Intervention for Registered Dietitians on Resilience, Burnout and Stress - A Cluster Randomised Control Trial
- ClinicalTrials.gov ID
- NCT07155512
- Acronym / sponsor ID
- FMHS 70-1123
- Keywords
- Registered Dietitian, Mindfulness, Randomised control trial, Resilience, Burnout, Stress, Mindfulness based intervention, Health personnel
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 30 participants (actual)
- Lead sponsor
- University of NottinghamUniversity, hospital or other
- Study start
- 8 Mar 2024 (actual)
- Primary completion
- 19 Jun 2025 (actual)
- Study completion
- 19 Jun 2025 (actual)
- First posted
- 4 Sep 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this randomised control trial is to find out whether a mindfulness based intervention can improve mental well-being for Registered Dietitians (RD) in the UK. The main question it aims to answer is:
Can a mindfulness based intervention improve resilience amongst UK RDs?
Can a mindfulness based intervention reduce stress and burnout amongst UK RDs?
Researchers will compare participants who attend a structured mindfulness based intervention with a waitlist control group to see if there is a difference in outcome measures between the groups before the intervention, immediately after, 3 months after and 6 months after.
Participants in the intervention group will be invited to an online mindfulness course that was written especially for this study. Participants in both groups will be asked to complete surveys before the intervention, immediately after, 3 months after and 6 months after. Participants in the intervention group will also be invited to participate in a one to one interview to discuss their experiences, barriers and facilitators to mindfulness in dietetic practice.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Mindfulness based intervention | Experimental | Behavioral: Mindfulness based interventionMindfulness based intervention (delivered synchronous online) |
| Waitlist control group | No intervention | –No intervention provided during the data collection period. Mindfulness based intervention delivered after data collection period. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- A Registered Dietitian currently practicing in the UK
- Willing and able to participate in 4 x 50 minute CPD sessions relating to mindfulness in dietetic practice (one session per week)
- Willing and able to complete all of the surveys (pre-intervention, immediately post, 3 months post and 6 months post intervention)
Key exclusion criteria (2 listed)
- A diagnosis of a psychotic condition
- A diagnosis of epilepsy or asthma that is not well controlled
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Mindfulness based interventionA mindfulness intervention was designed especially for this study and delivered by a RD also qualified as a mindfulness teacher. The intervention was delivered synchronously online and consisted of 4 x 50 minute sessions delivered across 4 weeks. | Behavioural | Mindfulness based intervention |
Primary outcome
Resilience
Time frame: Baseline, immediately after intervention (at the end of the last session of the 4 week intervention), 3 months post intervention, 6 months post intervention
Measured using validated tool: Brief Resilience Scale. Scores range from 1-5. Higher scores = higher level of resilience. 1.00-2.99= Low resilience; 3.00-4.30 = Normal resilience; 4.31-5.00= High resilience.
2 secondary outcomes
Burnout
Time frame: Baseline, immediately post (this survey is administered at the end of the 4th and final session of the intervention, which was week 4), 3 months post, 6 months post intervention
Stress
Time frame: Baseline, immediately post intervention (this survey was given at the end of the 4th and final session of the intervention), 3 months post intervention, 6 months post intervention
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Sep 2025.
- Individual participant dataSharing planned: Yes. Data collected in respect of 3 outcomes measured (resilience, burnout and stress) can be shared if required.
Related trials for Resilience, Psychological
Not yet recruiting
Effects of Art-Based Group Reminiscence Therapy on Resilience and Joy of Living in Older Adults
Resilience, Psychological, Joy of Living
Not yet recruiting
The Effect of Happiness Workshops on Nursing Students' Levels of Psychological Resilience
Psychological Resilience, Nursing Students
Active, not recruiting
Future School of Comprehensive Well-Being
Learning, Comprehensive Wellbeing
Recruiting
Study: Tea(m)Time - Strengthening the Team Resilience of Hospital Staff Through the Tea(m)Time Intervention
Resilience, Psychological, Personnel, Hospital
Recruiting
A Pragmatic Clinical Trial of the WE BEAT Well-Being Education Program in Adolescent Congenital Heart Disease: WE BEAT CHD Study
Patient-Reported Outcome Measures (PROMs), Pragmatic Trial
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Mindfulness based intervention in people with Resilience, Psychological and Burnout, Professional, run by University of Nottingham 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 3 inclusion and 2 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 4 Sep 2025. 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?
Resilience (time frame: Baseline, immediately after intervention (at the end of the last session of the 4 week intervention), 3 months post intervention, 6 months post intervention). 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 4 Sep 2025; AzTrials last refreshed its copy on 7 Nov 2026.