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NCT Number: NCT04899622

Mindfulness Online and Virtual Exercise (MOVE) Compared With Self-Management for Chronic Pain

The aim of this study is to assess the feasibility and acceptability of a combined Mindfulness Based Stress Reduction (MBSR) and exercise online programme compared to an online self-management guide. Pain management programmes are the recommended treatment for chronic pain, however a number of barriers to their widespread implementation have been identified including geographical distance from speciality programmes, functional disability limiting the mobility of people with CP and economic limitations(1). eHealth interventions have the potential to address a number of these barriers and recent reviews have reported reductions in pain(2), improved knowledge and understanding about chronic pain and chronic pain management, improved function(3) and improvements in quality of life(4) following eHealth interventions.

The intervention in this study will be delivered online. Participants will be randomly allocated to a combined MBSR and exercise programme (Group A) or an online self-management guide (Group B). Group A will take part in an 8 week live online weekly mindfulness sessions based on the Mindfulness Based Stress Reduction (MBSR) programme facilitated by a qualified mindfulness teacher, in addition to a supervised exercise classes led by a Physiotherapist. Group B will receive access to an 8 week online self-management guide containing 8 self-directed guides, which will be made available to participants biweekly.

Outcomes of feasibility and acceptability will be investigated in addition to a preliminary examination of between group clinical effects at baseline immediately post intervention and at a three month follow up, using validated patient reported outcome measures. In addition all participants will wear a Fitbit activity monitor for the duration of the eight-week interventions to capture activity measures. A qualitative study will also be conducted to gather participants' perceptions of the programme and its usefulness

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Key information

Conditions

Chronic Pain Behavior Motor Activity Neurologic Manifestations Pain Pathological Conditions, Signs and Symptoms Signs and Symptoms

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University College Dublin

Dublin, Ireland

About this study

This study is a parallel-groups, randomised-controlled, feasibility trial. Seventy-five participants aged 18 years and over, who have been diagnosed with a chronic pain condition by a Consultant in Pain Medicine or a General Practitioner will be recruited to the feasibility study. Participants will be individually randomised to one of two interventions. Group A will take part in live online weekly mindfulness sessions based on the Mindfulness Based Stress Reduction (MBSR) programme facilitated by a qualified mindfulness teacher, in addition to supervised exercise classes led by a Physiotherapist. The combined 3 hour intervention (2 hours MBSR, 1 hour exercise) will take place one day per week for 8 weeks. Group B will receive access to an 8 week online self-management guide containing 8 self-directed guides, with the material released biweekly.

The key outcomes measures will include; (1) recruitment rates, eligibility rates, willingness to be randomised; (2) feasibility and acceptability of data collection instruments and procedures; (3) intervention adherence, engagement and attrition rates; (4) feasibility and acceptability of the interventions and; (5) participants' subjective perceptions of the programmes.

The study will also include a preliminary examination of between group clinical effects at baseline, immediately post intervention and at a three month follow up, using the following validated patient reported outcome measures; Pain Self-Efficacy Questionnaire, Brief Pain Inventory, Pain Catastrophizing Scale, Generalised Anxiety Depression Assessment, Patient Health Questionnaire-9, Pain Disability Index, Fear Avoidance Belief Questionnaire, Short-Form-36 Health Survey, Patient Global Impression of Change Scale and measure of treatment satisfaction adapted from the Client Satisfaction Questionnaire (CSQ-8).

Physical activity levels (average daily step count, distance travelled and active minutes) will be measured for all participants using Fitbit Charge 4 activity monitors for the duration of the eight-week intervention period.

Analyses of the feasibility study will primarily be descriptive and will address the outcomes relating to the feasibility and acceptability of the interventions and the procedures of the study. Between-group comparisons of clinical treatment effects will be descriptive and exploratory to consider the viability of the combined MBSR and exercise intervention that may warrant further exploration in a fully powered RCT.

A sample of participants will be invited to attend focus groups where semi-structured interviews will be conducted with the aim of gathering information on the participants' subjective perceptions of the programme and its usefulness.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

•. Aged >18 years

  • Diagnosis of chronic pain by a Consultant in Pain Medicine or General Practitioner
  • Presence of pain NRS ≥ 3 of greater than three months' duration
  • Ability to provide informed consent
  • Ability to communicate in English and understand English

Exclusion criteria

  • Need for further diagnostic evaluation (determined by doctor)
  • Presence of any contraindications to participation in an exercise programme E.g. severe shortness of breath at rest, angina, uncontrolled diabetes or epilepsy, recent (previous 3 weeks) myocardial infarction, pulmonary embolism, deep vein thrombosis or asthma attack.
  • Presence of active cancer
  • Concurrent participation (or in the previous 3 months) with any form of psychological, physiotherapy or supervised exercise in addition to the study intervention.
  • Presence of substance misuse (diagnosed by the Pain Consultant/GP).
  • Inability to take part in an online exercise programme
  • Standard MBSR exclusion criteria

Treatment and study plan

MBSR

Behavioral

Participants will attend weekly online classes (two hours duration) of MBSR for eight weeks. The classes will be delivered live online to groups of up to fifteen participants and will be led by Mindfulness instructors with MSc degrees in Mindfulness Based Interventions. The programme content will be based on the standard MBSR programme and is tailored towards key concerns and difficulties experienced by individuals with chronic pain.

Exercise

Behavioral

Participants will attend weekly classes of supervised classes (1 hour) for eight weeks, following the MBSR class. The exercise class will be delivered live online to the group by an experienced Physiotherapist and will consist of a range of flexibility and strengthening exercises which will be advanced every two weeks for the duration of the eight week programme. The exercises will also be available in video format on the mobile application "Physitrack" which each participant will be invited to download. This will allow the participants to review the exercises between sessions, record online if they have completed each exercise and in addition rate their pain experience while completing the exercises.

Online Self-Management Guide

Behavioral

Participants will receive standard evidence based self-guided information which they will access independently via the members area of the study website. This 'Online Self-Management Guide' will consist of eight categories of self-management; (1) What is chronic pain? (2) Chronic pain and nutrition (3) Sleep issues with chronic pain (4) Activity and exercise (5) Pacing (6) Using a pain diary (7) Relaxation and mindfulness and (8) Course summary. The information will be presented in the form of general text, links to online resources and videos. The information in this area will be updated biweekly during the eight week programme with the participants receiving bi-weekly email reminders.

Primary outcomes

  1. Number of eligible participants identified per programme

    Time frame: Baseline

    Prior to each programme the number of eligible participants will be recorded by the primary researcher

  2. Number of eligible participants recruited per programme

    Time frame: Baseline

    Prior to each programme the number of eligible participants who are recruited will be recorded by the primary researcher

  3. Reasons for non-participation

    Time frame: Baseline

    This measure will be recorded by the primary researcher when screening participants

  4. Number of participants who complete the study

    Time frame: immediately post intervention (8 weeks from baseline)

    The number of participants that complete >50% of the online classes programme

  5. Adherence to completion of baseline patient reported outcome measures

    Time frame: Baseline

    Numbers of participants completing > 90% of baseline patient reported outcome measures

  6. Adherence to completion of immediate follow-up patient reported outcome measures

    Time frame: Immediately post intervention (8 weeks from baseline)

    Numbers of participants completing > 90% of follow-up patient reported outcome measures

  7. Adherence to completion of long term follow-up patient reported outcome measures

    Time frame: 3 months post intervention (20 weeks from baseline)

    Numbers of participants completing > 90% of follow-up patient reported outcome measures

  8. Interaction with online self-management guide

    Time frame: Immediately post intervention (8 weeks from baseline)

    The study website analytics will measure the number of views that each element of the online guide receives (Group B)

  9. Treatment Acceptability (Satisfaction assessed by Client Satisfaction Questionnaire-8)

    Time frame: Immediately post intervention (8 weeks from baseline)

    Patient satisfaction with treatment will be measured with an adapted version of the Client Satisfaction Questionnaire-8. Responses are scored from 1-4, and the possible total scores range from 8 to 32. Higher scores indicate greater satisfaction.

  10. Interface usability

    Time frame: immediately post intervention (8 weeks from baseline)

    Measures of website usability will be investigated with an adapted System Usability Scale (SUS) Scores range from 10-50. Higher scores indicated greater ease of usability.

Secondary outcomes

  1. Change in pain self-efficacy measured with the Pain Self-Efficacy Questionnaire

    Time frame: immediately post intervention (8 weeks from baseline) and 12 week follow up (20 weeks from baseline)

    The Pain Self-Efficacy Questionnaire is a ten item questionnaire which assesses an individual's confidence in their ability to perform a variety of activities or tasks despite pain. Scores can range from 0 - 60. Higher scores represent lower confidence to function with pain.

  2. Change in symptoms of anxiety measured with the Generalized Anxiety Disorder Assessment

    Time frame: immediately post intervention (8 weeks from baseline) and 12 week follow up (20 weeks from baseline)

    The Generalized Anxiety Disorder 7 assesses symptoms of anxiety experienced during the last two weeks. The total score for the seven items ranges from 0 to 21. Higher scores represent higher levels of anxiety.

  3. Changes in symptoms of depression measured with the Patient Health Questionnaire 9

    Time frame: immediately post intervention (8 weeks from baseline) and 12 week follow up (20 weeks from baseline)

    Symptoms of depression will be assessed using the Patient Health Questionnaire 9, which is a nine-item questionnaire generating scores ranging from 0-27. Higher scores indicate increased severity of depression.

  4. Changes in pain severity and pain interference measured with the Brief Pain Inventory-Composite pain score

    Time frame: immediately post intervention (8 weeks from baseline) and 12 week follow up (20 weeks from baseline)

    Pain severity will be measured using the pain severity subscale of the Brief Pain Inventory. Pain interference will be measured using the interference subscale of the Brief Pain Inventory, which measures the extent to which pain interferes with functions such as general activity, walking ability, normal work, mood, relationships with people, enjoyment of life and sleep. For each scale, the total score is the average of all items (range, 0-10), where a higher score indicates greater severity and more interference.

  5. Changes in the impact of pain on individuals life participation measured with the Pain Disability Index

    Time frame: immediately post intervention (8 weeks from baseline) and 12 week follow up (20 weeks from baseline)

    The Pain Disability Index measure asks patients to rate how much pain interferes in seven areas of life activity: family/home, recreation, social, occupation, sexual, self-care and life-support. Total score ranges from 0-70. The higher the score the greater the person's disability due to pain.

  6. Changes in fear avoidance of physical activity measured with the Fear Avoidance Belief Questionnaire.

    Time frame: immediately post intervention (8 weeks from baseline) and 12 week follow up (20 weeks from baseline)

    The Fear Avoidance Belief Questionnaire measures patients' fear of pain and consequent avoidance of physical activity because of their fear. The questionnaire consists of 16 items in which a patient rates their agreement with each statement on a 7-point Likert scale. The scores range from 0-96; higher scores indicates increased fear avoidance behaviours.

  7. Change in pain catastrophising measured with the Pain Catastrophising Scale.

    Time frame: immediately post intervention (8 weeks from baseline) and 12 week follow up (20 weeks from baseline)

    The Pain Catastrophising Scale is a 13-item instrument designed to assess catastrophic thinking in relation to pain. It yields a total score and three subscale scores assessing rumination, magnification and helplessness. Scores range from 0-52. Higher scores are associated with higher amounts of pain catastrophising.

  8. Change in quality of life measured with the Short Form-36 Health Survey

    Time frame: immediately post intervention (8 weeks from baseline) and 12 week follow up (20 weeks from baseline)

    The Short Form-36 Health Survey comprises of 36 questions which cover eight domains of general health. Scores range from 0-100. The lower the score the more disability.

  9. Patient Global Impression of Change Scale

    Time frame: immediately post intervention (8 weeks from baseline)

    The Patient Global Impression of Change Scale scale measures a patient's rating of overall improvement or lack thereof due to the intervention. It is a 7 point scale depicting a patient's rating of overall improvement. Patients rate their change as "very much improved," "much improved," "minimally improved," "no change," "minimally worse," "much worse," or "very much worse."

  10. Changes in step count (Fitbit)

    Time frame: immediately post intervention (8 weeks from baseline)

    Average weekly step count will be measured using a Fitbit Charge 4 activity monitor worn by participants for the eight weeks of the intervention.

  11. Changes in distance travelled (Fitbit)

    Time frame: immediately post intervention (8 weeks from baseline)

    Average weekly distance travelled will be measured using a Fitbit Charge 4 activity monitor worn by participants for the eight weeks of the intervention.

  12. Changes in active minutes (Fitbit)

    Time frame: immediately post intervention (8 weeks from baseline)

    Average active minutes will be measured using a Fitbit Charge 4 activity monitor worn by participants for the eight weeks of the intervention.

Sponsors and collaborators

Lead sponsor

Orla Deegan

Other

Collaborators

  • Mater Misericordiae University Hospital
  • University College Dublin

Registry information

Official study title

Mindfulness Combined With Virtual Exercise Online (MOVE) Compared With a Self-Management Guide for Adults With Chronic Pain: Study Protocol for a Feasibility Randomised Controlled Trial

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
May 24, 2021
Registry last updated
Oct 5, 2022

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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