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Applying an Osteopathic Intervention to Improve Mental Health Symptoms: a Mixed-methods Feasibility Study Protocol.

Applying an Osteopathic Intervention to Improve Mild to Moderate Mental Health

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05674071
Enrollment
32
Registered
2023-01-06
Start date
2022-12-20
Completion date
2023-08-01
Last updated
2023-11-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mental Health Issue

Brief summary

Applying an osteopathic intervention to improve mild to moderate mental health symptoms: a mixed-methods feasibility study protocol.

Detailed description

Introduction: Mental health services are stretched in the UK and in need of support. One approach that could improve mental health symptoms is osteopathy. Research suggests that osteopathy influences psychophysiological factors, which could lead to improvements in mental health. The first objective of this protocol is to investigate the feasibility and acceptability of four osteopathic interventions. A secondary aim is to evaluate the interventions' effectiveness in improving psychophysiological and mental health outcomes. Methods and analysis: This study will be an explanatory mixed-methods design. Participants will be 30 adults who have mild to moderate mental health symptoms and not experiencing any issues with pain. The feasibility and acceptability of the interventions will be the first primary outcome. Secondary outcomes will be physiological measures including heart rate variability (HRV), interoceptive accuracy (IAc) and blood pressure (BP). Psychological outcomes will also be measured by standardised questionnaires. These are being collected pre-and post-intervention. Additional outcomes will include recruitment rates and any adverse events that occur during the study. Participants will be randomised to one of four interventions. These are: high-velocity and articulation techniques (HVAT), soft-tissue massage (STM), craniosacral therapy (CST), and a combination of these three approaches. Participants will be interviewed about their experiences of the study and interventions to aid in assessing the feasibility and acceptability. Discussion: This study will assess the feasibility and acceptability of conducting osteopathic interventions for improving mental health outcomes. These results from this will help to inform the running of a future randomised controlled trial. The study will also be producing original data which could provide preliminary evidence whether osteopathic approaches are of benefit to individual's mental health, even if they are pain-free.

Interventions

BEHAVIORALArticulation/HVT

Osteopathy 1

BEHAVIORALSoft-tissue massage

Osteopathy 2

BEHAVIORALCraniosacral techniques

Osteopathy 3

BEHAVIORALCombination of the three interventions: HVT, soft-tissue and craniosacral techniques

This intervention will use a combination of the three interventions: HVT, soft-tissue and craniosacral techniques

Sponsors

Osteopathic Foundation
CollaboratorUNKNOWN
University College of Osteopathy
CollaboratorOTHER
Swansea University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Mild to moderate mental health symptoms as measured by DASS * Ability to read/write English.

Exclusion criteria

* No mental health symptoms or severe mental health symptoms (as measured by DASS) * acute or chronic pain

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of study recruitment3 monthsRecruitment rate
Feasibility of time to complete study3 monthsTime to complete questionnaires
Feasibility of study data collection3 monthsMissing data reported
Feasibility of assessing physiological measurements3 monthsTime to take physiological measurements
Acceptability of intervention to participants3 monthsFeedback from participants in qualitative interviews
Acceptability of intervention and risk factors3 monthsAdverse events reported

Secondary

MeasureTime frameDescription
Depression Anxiety and Stress Scale (DASS)3 monthsMeasure of depression, anxiety and stress. Scores range from 0-21 for each of the 3 sub scales and higher scores indicate greater levels of depression, anxiety or stress.
Positive and negative affect schedule (PANAS)3 monthsMeasure of positive and negative affect. Scores range from 10-50 for each of the 2 sub scales and higher scores indicate higher levels of positive and negative affect.
Acceptance and action questionnaire (AAQ)3 monthsMeasure of psychological inflexibility. Scores range from 7-49 and higher scores indicate higher levels of psychological inflexibility.
Self as context scale (SACS)3 monthsMeasure of self-as-context and perspective taking. Has two sub scales of centering and transcending ranging from 5-35, with higher scores indicating greater levels of these.
Multidimensional Assessment of Interoceptive Awareness (MAIA)3 monthsMeasure of interoceptive awareness. Uses 8 sub scales and higher scores indicate greater levels of each domain of interoceptive awareness.
Heart rate variability3 monthsMeasure by time-domain: root mean square of successive interval differences (RMSSD) and frequency domain: low frequency to high frequency ratio.
Interoceptive accuracy3 monthsMeasured using heartbeat detection task
Blood pressure3 monthsParticipants blood pressure will be recorded according to NICE guidelines

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026