Ignite Creation Date:
2024-05-06 @ 9:01 AM
Last Modification Date:
2024-10-26 @ 12:08 PM
Study NCT ID:
NCT02881411
Status:
COMPLETED
Last Update Posted:
2017-07-14
First Post:
2016-08-10
Brief Title:
Self Soft Tissue Therapy for Fibromyalgia Syndrome
Sponsor:
University of the West of England
Organization:
University of the West of England
Study Overview
Official Title:
Self Soft Tissue Therapy for Fibromyalgia Syndrome Randomised Controlled Feasibility Study
Status:
COMPLETED
Status Verified Date:
2017-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The main aims of this preliminary research are to determine if combined self-soft tissue therapy SSTT alongside an established 6 week FMS Coping Skills Programme FCSP is a feasible and acceptable treatment approach for FMS All participants on the six week FCSP will be randomly allocated to a control FMS Coping Skills Programme or intervention group FMS Coping Skills Programme plus SSTT All participants will be assessed for outcome measurements at the start of the feasibility study at six weeks and three months after completion
This feasibility study hypothesis is that the SST approach will be acceptable to FMS patients and that the combined 6 week FCSP hands off and SSTT hands on will be beneficial This feasibility study will inform a larger randomized controlled trial RCT on this combined treatment approach to FMS
This feasibility study hypothesis is that the SST approach will be acceptable to FMS patients and that the combined 6 week FCSP hands off and SSTT hands on will be beneficial This feasibility study will inform a larger randomized controlled trial RCT on this combined treatment approach to FMS
Detailed Description:
AIMS OBJECTIVES
The main aims of this preliminary research are
1 To determine the feasibility of conducting a future larger study in terms of recruitment randomisation estimates of effect size study protocol and procedure intervention and outcome acceptability
2 To determine if combining SSTT MTrP therapy as an adjunct to the presently only provided usual care of hands off rehabilitation and self-management programme is feasible and acceptable to participants in this combined treatment approach to FMS
METHOD
The multidisciplinary team includes researchers and health professionals who are actively involved in musculoskeletal therapy and research This current randomised controlled feasibility study is supported by internal funding from the Faculty of Health Applied Sciences University of the West of England UWE Bristol Ethics approval from NHS ethicsIRAS has been obtained
Participant be identification and recruitment Participants will be identified and recruited from those FMS patients enrolled on the 6 week FCSP in the Royal National Hospital for Rheumatic Diseases RNHRD out-patients department All enrolled patients on the FCSP will be emailed and sent out an invitation letter and information sheet by the RNHRD admin and clinical team requesting participation in the feasibility study
Prior to primary collection of data all participants sign an informed consent form Participants will undergo a screening for inclusionexclusion criteria will provide demographic information and complete a general health screening survey
Randomisation- All participants will be randomly allocated to either a control or intervention group by an independent researcher using block randomisation utilising an online randomisation tool This method involves creating a table using two number sets The randomiser ensures each group appears an equal number of times whilst simultaneously randomly allocating participants to each group The randomisation order will be performed by the co-researcher who will prepare opaque envelopes that can be opened at a relevant point in the process
Control Group - Participants will undertake the 6 FCSP only The FCSP is a non-pharmacological multidisciplinary exercise and education group programme Its main aims are to provide condition-specific patient centred self-management education and advice in line with national drivers for long-term conditions and international FMS clinical guidelines
All group participants are screened prior to acceptance onto the FCSP and must have a diagnosis of fibromyalgia using the ACR 1990 or 2010 criteria Patients with co-morbidities are accepted Core components of the 6 week FCSP include goal-setting pacing hydrotherapy exercise and dietary advice There is one face-to-face review session three months after the taught component of the FCSP is completed
Patient reported outcome measures PROMS are collected from participants at three time-points start of course end of course and three months post course These are inputted onto a clinical database and analysed to measure clinical progress on an individual basis
Intervention Group - Participants in this group will undertake the 6 week FCSP plus SSTT myofascial trigger point MTrP therapy initially TrP pressure release performed by the researcher and then also taught a SSTT home programme The specific form of soft tissue therapy used in this feasibility study is MTrP therapy as used in a case series on triceps surae dysfunction as described in the protocol below This protocol is adapted for patients with FMS and will be administered by the researcher for only two sessions which will include training to teach the participant how to do SSTT on themselves All participants in the control group will receive an advice booklet for SSTT
Researcher TrP pressure release intervention- Lower legfoot- The participants will be positioned prone with the knee extended for TrP pressure release on the gastrocnemius and knee flexed for the soleus While still in prone TrP pressure release will also be used on the medial plantar aspect of the foot specifically quadratus plantar and abductor halluces TrP pressure release employing the barrier release concept will be used The researcher will slowly apply increasing thumb pressure on the soleus or gastrocnemius MTrPs until the first increase in tissue resistance is felt barrier Pressure will initially be perceived as tender or mildly painful but participants will be instructed to notify the researcher to stop if the procedure is not tolerable Pressure will be maintained until a release in muscle tension or until the participant feels no tenderness or pain only related to the thumb pressure On releasing the pressure the researcher will apply a passive stretch to the affected calf muscle to facilitate maintenance of the gained muscle length On subsequent visits TrP pressure release will be progressed while rocking or facilitating the ankle into greater dorsiflexion and will be applied to the hamstrings while flexing and extending the knee Participants will be warned about possible mild post treatment soreness mild ache which may last up to 24 hours but will not interfere with day to day function
ForearmHand- Exactly the same TrP pressure release protocol will be used All participants will be seated with the forearm resting on a plinth with researcher and participant facing each other The thenar and hypothenar muscles wrist extensor and flexor muscles will receive TrP pressure release and stretching
Self soft tissue therapy SSTT- participants will be advised on self treatment and shown the technique on identified active or latent MTrPs in the lower legfoot or forearmhand Participants will be shown varying techniques including self-massage use of a tennis ball or foam roller All participants will be advised to do SSTT at least once a day and advised to stop SSTT if symptoms are increased
Stretching programme - stretching is advised post SSTT of MTrPs as part of a home exercise programme A standardised home stretching protocol will be issued and detailed in the advice booklet including demonstration of the stretching techniques and advice on dosage A full description and demonstration will be given to participants No specific time will be given for the stretching protocol as the evidence is inconclusive on the duration of static stretch needed to produce benefit
Data management and analysis- Data will be analysed by the PI and co-researcher in an office at the University of the West of England Statistical Package for the Social Sciences SPSS version 200 will be used to analyse the data using descriptive mean standard deviation and range of scores at the initial and follow up sessions The results of the additional FCSP FMS PROMS and criteria for FMS diagnosis-Widespread Pain IndexSymptom Severity Score plus tenderness in 18 tender point sites will also be analysed for differences between groups In line with the aims of this feasibility study no inferential statistics will be employed
Sampling frame-
As this is feasibility study no sample size or power calculation has been conducted The aim is to recruit 20 patients enough to meet the aims of a feasibility study and being sufficient to provide estimates of variability between the control and intervention groups All potential participants to be screened and accepted if they meet the inclusionexclusion criteria
Confidentiality Anonymity- Any data produced from the feasibility study will be anonymised therefore any identifying details will be replaced numerically All data will be analysed and downloaded on a password protected computer at the University of the West of England
Data handling and Record Keeping- The CI and PI will be responsible for data collection recording and quality Anonymised collected data from each participant will be analysed and downloaded on a password protected computer at the University of the West of England Data will be collected and retained in accordance with the Data Protection Act 1998 Back-up copies of electronic data will be made regularly onto a CD All source documents will be retained for a period of 5 years following the end of the study
Addressing Consent Withdrawal- Consent- Consent will be addressed via an informed consent form that will be given to all participants a week before data collection and signed prior to collection of data A full explanation and opportunity to ask questions prior and during data collection will be afforded to all participants
Withdrawal- Participants are completely free to abstain or withdraw from the feasibility study at any time during the process of data collection
Risk Risk Management- Participants will be invited to participate in the feasibility study Each participant will have the option to participate or opt out Participants futures will not be affected in any way by their decision to take part or not There will not be any physical psychological social legal or economic risks for participants to participate in the feasibility study There will be no additional risks to the researchers or other people impacted by this study as a consequence of undertaking this proposal that are greater than those encountered in normal day-to-day life
Access to source data- Direct access to the source data and documents will be permitted for monitoring audits Research Ethics Committees and review
Safety Assessments and Monitoring- The project management committee will consist of the research team Dr Rob Grieve Sandi Derham and Julie Russell who will meet regularly to assess the study This study will be monitored and audited in accordance with UWE policy
Other Ethical Considerations- Apart from the already mentioned possible mild discomfort participants will have to make an effort to attend the sessions and do the SSTT home programme
The main aims of this preliminary research are
1 To determine the feasibility of conducting a future larger study in terms of recruitment randomisation estimates of effect size study protocol and procedure intervention and outcome acceptability
2 To determine if combining SSTT MTrP therapy as an adjunct to the presently only provided usual care of hands off rehabilitation and self-management programme is feasible and acceptable to participants in this combined treatment approach to FMS
METHOD
The multidisciplinary team includes researchers and health professionals who are actively involved in musculoskeletal therapy and research This current randomised controlled feasibility study is supported by internal funding from the Faculty of Health Applied Sciences University of the West of England UWE Bristol Ethics approval from NHS ethicsIRAS has been obtained
Participant be identification and recruitment Participants will be identified and recruited from those FMS patients enrolled on the 6 week FCSP in the Royal National Hospital for Rheumatic Diseases RNHRD out-patients department All enrolled patients on the FCSP will be emailed and sent out an invitation letter and information sheet by the RNHRD admin and clinical team requesting participation in the feasibility study
Prior to primary collection of data all participants sign an informed consent form Participants will undergo a screening for inclusionexclusion criteria will provide demographic information and complete a general health screening survey
Randomisation- All participants will be randomly allocated to either a control or intervention group by an independent researcher using block randomisation utilising an online randomisation tool This method involves creating a table using two number sets The randomiser ensures each group appears an equal number of times whilst simultaneously randomly allocating participants to each group The randomisation order will be performed by the co-researcher who will prepare opaque envelopes that can be opened at a relevant point in the process
Control Group - Participants will undertake the 6 FCSP only The FCSP is a non-pharmacological multidisciplinary exercise and education group programme Its main aims are to provide condition-specific patient centred self-management education and advice in line with national drivers for long-term conditions and international FMS clinical guidelines
All group participants are screened prior to acceptance onto the FCSP and must have a diagnosis of fibromyalgia using the ACR 1990 or 2010 criteria Patients with co-morbidities are accepted Core components of the 6 week FCSP include goal-setting pacing hydrotherapy exercise and dietary advice There is one face-to-face review session three months after the taught component of the FCSP is completed
Patient reported outcome measures PROMS are collected from participants at three time-points start of course end of course and three months post course These are inputted onto a clinical database and analysed to measure clinical progress on an individual basis
Intervention Group - Participants in this group will undertake the 6 week FCSP plus SSTT myofascial trigger point MTrP therapy initially TrP pressure release performed by the researcher and then also taught a SSTT home programme The specific form of soft tissue therapy used in this feasibility study is MTrP therapy as used in a case series on triceps surae dysfunction as described in the protocol below This protocol is adapted for patients with FMS and will be administered by the researcher for only two sessions which will include training to teach the participant how to do SSTT on themselves All participants in the control group will receive an advice booklet for SSTT
Researcher TrP pressure release intervention- Lower legfoot- The participants will be positioned prone with the knee extended for TrP pressure release on the gastrocnemius and knee flexed for the soleus While still in prone TrP pressure release will also be used on the medial plantar aspect of the foot specifically quadratus plantar and abductor halluces TrP pressure release employing the barrier release concept will be used The researcher will slowly apply increasing thumb pressure on the soleus or gastrocnemius MTrPs until the first increase in tissue resistance is felt barrier Pressure will initially be perceived as tender or mildly painful but participants will be instructed to notify the researcher to stop if the procedure is not tolerable Pressure will be maintained until a release in muscle tension or until the participant feels no tenderness or pain only related to the thumb pressure On releasing the pressure the researcher will apply a passive stretch to the affected calf muscle to facilitate maintenance of the gained muscle length On subsequent visits TrP pressure release will be progressed while rocking or facilitating the ankle into greater dorsiflexion and will be applied to the hamstrings while flexing and extending the knee Participants will be warned about possible mild post treatment soreness mild ache which may last up to 24 hours but will not interfere with day to day function
ForearmHand- Exactly the same TrP pressure release protocol will be used All participants will be seated with the forearm resting on a plinth with researcher and participant facing each other The thenar and hypothenar muscles wrist extensor and flexor muscles will receive TrP pressure release and stretching
Self soft tissue therapy SSTT- participants will be advised on self treatment and shown the technique on identified active or latent MTrPs in the lower legfoot or forearmhand Participants will be shown varying techniques including self-massage use of a tennis ball or foam roller All participants will be advised to do SSTT at least once a day and advised to stop SSTT if symptoms are increased
Stretching programme - stretching is advised post SSTT of MTrPs as part of a home exercise programme A standardised home stretching protocol will be issued and detailed in the advice booklet including demonstration of the stretching techniques and advice on dosage A full description and demonstration will be given to participants No specific time will be given for the stretching protocol as the evidence is inconclusive on the duration of static stretch needed to produce benefit
Data management and analysis- Data will be analysed by the PI and co-researcher in an office at the University of the West of England Statistical Package for the Social Sciences SPSS version 200 will be used to analyse the data using descriptive mean standard deviation and range of scores at the initial and follow up sessions The results of the additional FCSP FMS PROMS and criteria for FMS diagnosis-Widespread Pain IndexSymptom Severity Score plus tenderness in 18 tender point sites will also be analysed for differences between groups In line with the aims of this feasibility study no inferential statistics will be employed
Sampling frame-
As this is feasibility study no sample size or power calculation has been conducted The aim is to recruit 20 patients enough to meet the aims of a feasibility study and being sufficient to provide estimates of variability between the control and intervention groups All potential participants to be screened and accepted if they meet the inclusionexclusion criteria
Confidentiality Anonymity- Any data produced from the feasibility study will be anonymised therefore any identifying details will be replaced numerically All data will be analysed and downloaded on a password protected computer at the University of the West of England
Data handling and Record Keeping- The CI and PI will be responsible for data collection recording and quality Anonymised collected data from each participant will be analysed and downloaded on a password protected computer at the University of the West of England Data will be collected and retained in accordance with the Data Protection Act 1998 Back-up copies of electronic data will be made regularly onto a CD All source documents will be retained for a period of 5 years following the end of the study
Addressing Consent Withdrawal- Consent- Consent will be addressed via an informed consent form that will be given to all participants a week before data collection and signed prior to collection of data A full explanation and opportunity to ask questions prior and during data collection will be afforded to all participants
Withdrawal- Participants are completely free to abstain or withdraw from the feasibility study at any time during the process of data collection
Risk Risk Management- Participants will be invited to participate in the feasibility study Each participant will have the option to participate or opt out Participants futures will not be affected in any way by their decision to take part or not There will not be any physical psychological social legal or economic risks for participants to participate in the feasibility study There will be no additional risks to the researchers or other people impacted by this study as a consequence of undertaking this proposal that are greater than those encountered in normal day-to-day life
Access to source data- Direct access to the source data and documents will be permitted for monitoring audits Research Ethics Committees and review
Safety Assessments and Monitoring- The project management committee will consist of the research team Dr Rob Grieve Sandi Derham and Julie Russell who will meet regularly to assess the study This study will be monitored and audited in accordance with UWE policy
Other Ethical Considerations- Apart from the already mentioned possible mild discomfort participants will have to make an effort to attend the sessions and do the SSTT home programme
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None