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Physical and Psychological Changes in CRPS Patients Undergoing Multimodal Rehabilitation

Primary Purpose

Complex Regional Pain Syndromes

Status
Active
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
Multimodal rehabilitation
Sponsored by
National Institute of Geriatrics, Rheumatology and Rehabilitation, Poland
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Complex Regional Pain Syndromes focused on measuring CRPS, cognitive functions, physical therapy, pain, Graded Motor Imagery, mirror therapy, rehabilitation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Clinical diagnosis of CRPS (or equivalent); MMSE >24 points; Has signed an informed consent to the study. Exclusion Criteria: MMSE ≤24 points; Inability to perform scheduled tasks (multimodal rehabilitation program).

Sites / Locations

  • National Institute of Geriatrics, Rheumatology and Rehabilitation

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

CRPS

Healthy Control

Arm Description

Participants meeting inclusion and exclusion criteria undergoing 4-week multimodal rehabilitation, undergoing assessment at baseline and at 4 weeks.

Participants matched according to sex, age and education to experimental arm, undergoing psychological assessment at baseline and at 4 weeks.

Outcomes

Primary Outcome Measures

Mean change from baseline in Reproduction score on the Rey's Complex Figure Test (RCFT) score at 4 weeks.
The RCFT is a task-based test assessing visual-spatial abilities. Reproduction score measures learning and planning on visual material. Possible scores range from 0 (significant deficit) to 36 (highest possible score). Change = (week 4 score - baseline score).

Secondary Outcome Measures

Mean change from baseline in Copy score on the Rey's Complex Figure Test (RCFT) score at 4 weeks.
The RCFT is a task-based test assessing visual-spatial abilities. Copy score measures planning on visual material. Possible scores range from 0 (significant deficit) to 36 (highest possible score). Change = (week 4 score - baseline score).
Mean change from baseline in pain score on the Numeric Rating Scale (NRS) at 4 weeks
The NRS is a self-reported instrument assessing average pain intensity over the past 24 hour period. Possible scores range from 0 (no pain) to 10 (worst possible pain). Change = (week 4 score - baseline score).
Mean change from baseline in Disabilities of the Arm, Shoulder, and Hand Questionnaire (DASH) at 4 weeks in Participants with upper extremity CRPS
The DASH is a self-reported instrument assessing ability to perform certain upper extremity activities. Possible scores range from 0 (no disability) to 100 (complete disability). Change = (week 4 score - baseline score).
Mean change from baseline in Lower Extremity Functional Scale (LEFS) at 4 weeks in Participants with lower extremity CRPS
The LEFS is a self-reported instrument assessing ability to perform certain lower extremity activities. Possible scores range from 0 (complete disability) to 80 (no disability). Change = (week 4 score - baseline score).
Number of Participants meeting the Budapest Criteria for CRPS at baseline as percent of Participants in the CRPS arm
The Budapest Criteria are a set of clinical criteria used to diagnose CRPS. Possible outcomes include: CRPS-I, CRPS-II, CRPS-RSF, not meeting Budapest Criteria. Number = ((number of CRPS-I + number of CRPS-II + number of CRPS-RSF) / total Participants in CRPS arm) * 100%.
Mean change from baseline in active range of motion (aROM) of affected joint at 4 weeks
The aROM is a clinical measure calculated as an angle between extreme positions of a joint. Possible scores range from 0° (no motion) to 360° (full rotation). Change = ((week 4 score / baseline score) * 100%).
Mean change from baseline in Central Sensitization Inventory (CSI) part A at 4 weeks
The CSI is a self-reported instrument assessing overlapping health-related symptom dimensions of central sensitization. Possible scores range from 0 (subclinical) to 100 (extreme). Change = (week 4 score - baseline score).
Mean change from baseline in Short-Form McGill Pain Questionnaire (SF-MPQ) part A score at 4 weeks
The SF-MPQ is a self-reported instrument assessing different types of pain. Possible scores range from 0 (no pain) to 45 (severe pain). Change = (week 4 score - baseline score).
Mean change from baseline in PainDetect Questionnaire (PDQ) score at 4 weeks
The PDQ is a self-reported instrument assessing neuropathic pain. Possible scores range from -1 (neuropathic component <15%) to 38 (neuropathic component >90%). Change = (week 4 score - baseline score).
Mean change from baseline in Diverting Attention score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
The CSQ is a self-reported instrument assessing different pain coping strategies. The Diverting Attention score measures the use of attention diversion as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 36 (strategy significantly engaged). Change = (week 4 score - baseline score).
Mean change from baseline in Reinterpreting Pain Sensations score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
The CSQ is a self-reported instrument assessing different pain coping strategies. The Reinterpreting Pain Sensations score measures the use of pain sensation reinterpretation as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 36 (strategy significantly engaged). Change = (week 4 score - baseline score).
Mean change from baseline in Catastrophizing score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
The CSQ is a self-reported instrument assessing different pain coping strategies. The Catastrophizing score measures the use of catastrophising as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 36 (strategy significantly engaged). Change = (week 4 score - baseline score).
Mean change from baseline in Ignoring Sensation score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
The CSQ is a self-reported instrument assessing different pain coping strategies. The Ignoring Sensation score measures the use of ignoring pain sensation as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 36 (strategy significantly engaged). Change = (week 4 score - baseline score).
Mean change from baseline in Praying or Hoping score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
The CSQ is a self-reported instrument assessing different pain coping strategies. The Praying or Hoping score measures the use of prayer and wishful thinking as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 36 (strategy significantly engaged). Change = (week 4 score - baseline score).
Mean change from baseline in Coping Self Statements score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
The CSQ is a self-reported instrument assessing different pain coping strategies. The Coping Self Statements score measures positive self-affirmations as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 36 (strategy significantly engaged). Change = (week 4 score - baseline score).
Mean change from baseline in Increased Behavioral Activity score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
The CSQ is a self-reported instrument assessing different pain coping strategies. The Increased Behavioral Activity score measures the use of behavioral activity increase as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 36 (strategy significantly engaged). Change = (week 4 score - baseline score).
Mean change from baseline in Control Over Pain score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
The CSQ is a self-reported instrument assessing different pain coping strategies. The Control Over Pain score measures the notion of control over pain as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 6 (strategy significantly engaged). Change = (week 4 score - baseline score).
Mean change from baseline in Ability to Decrease Pain score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
The CSQ is a self-reported instrument assessing different pain coping strategies. The Ability to Decrease Pain score measures the notion of being able to decrease pain as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 6 (strategy significantly engaged). Change = (week 4 score - baseline score).
Mean score on the Mini-Mental State Examination (MMSE) at baseline.
The MMSE is a clinician-reported screening test assessing general cognitive functioning. Possible scores range from 0 (severe cognitive deficit) to 30 (no cognitive deficit).
Mean change from baseline in Total Number Correct score in Benton Visual Retention Test (BVRT) at 4 weeks.
The BVRT is a task-based test assessing visual-spatial working memory and visual-spatial abilities. Total Number Correct score counts correct answers. Possible scores range from 0 (significant deficit) to 10 (highest possible score). Change = (week 4 score - baseline score).
Mean change from baseline in Number of Errors score in the Benton Visual Retention Test (BVRT) at 4 weeks.
The BVRT is a task-based test assessing visual-spatial working memory and visual-spatial abilities. Number of Errors score counts wrong answers. Possible scores range from 0 (best possible score) to 10 (worst possible score). Change = (week 4 score - baseline score).
Mean change from baseline in Digit Span (DS) score in Wechsler's Adult Intelligence Scale Revised (WAIS-R) at 4 weeks.
WAIS-R is a task-based test assessing intelligence. The DS score measures attention and working memory. Possible scores range from 0 (significant deficit) to 28 (highest possible score). Change = (week 4 score - baseline score).
Mean change from baseline in Beck Depression Inventory - II (BDI-II) score at 4 weeks.
The BDI-II is a self-reported questionnaire assessing depression severity. Possible scores range from 0 (no depression) to 66 (severe depression). Change = (week 4 score - baseline score).
Mean change from baseline in Speed of Work score in the Attention and Perceptiveness Test (TUS) - at 4 weeks.
The TUS is a task-based test assessing attention. Speed of Work measures number of tasks completed in a fixed amount of time. Possible scores range from 0 (lowest possible speed) to 972 (highest possible speed). Change = (week 4 score - baseline score).
Mean change from baseline in Number of Mistakes score in the Attention and Perceptiveness Test (TUS) at 4 weeks.
The TUS is a task-based test assessing attention. Number of Mistakes score measures resistance to distraction. Possible scores range from 0 (perfect score) to 972 (worst possible score). Change = (week 4 score - baseline score).
Mean change from baseline in Number of Omissions in the Attention and Perceptiveness Test (TUS) at 4 weeks.
The TUS is a task-based test assessing attention. Number of Omissions score measures resistance to distraction. Possible scores range from 0 (perfect score) to 349 (worst possible score). Change = (week 4 score - baseline score).
Mean change from baseline in execution time in the Color-Trials Test part 1 (CTT-1) at 4 weeks.
The CTT-1 is a task-based test assessing psychomotor speed in time (seconds). Possible scores range from 0s (impossibly fast) to infinite time (unable to complete). Change = (week 4 time in seconds - baseline time in seconds).
Mean change from baseline in shifting attention score on the Color-Trials Test part 2 (CTT-2) at 4 weeks.
The CTT-2 is a task-based test assessing shifting attention in time (seconds). Possible scores range from 0s (impossibly fast) to infinite time (unable to complete task). Change = (week 4 time in seconds - baseline time in seconds).

Full Information

First Posted
January 13, 2023
Last Updated
January 13, 2023
Sponsor
National Institute of Geriatrics, Rheumatology and Rehabilitation, Poland
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1. Study Identification

Unique Protocol Identification Number
NCT05696587
Brief Title
Physical and Psychological Changes in CRPS Patients Undergoing Multimodal Rehabilitation
Official Title
Physical and Psychological Changes in Complex Regional Pain Syndrome (CRPS) Patients Undergoing Multimodal Rehabilitation
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
October 10, 2021 (Actual)
Primary Completion Date
January 2023 (Anticipated)
Study Completion Date
January 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Institute of Geriatrics, Rheumatology and Rehabilitation, Poland

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this clinical trial is to learn about cognitive changes during rehabilitation in CRPS patients. The main questions it aims to answer are: What are the cognitive changes in CRPS? Do cognitive functions change during multimodal rehabilitation in CRPS? What is the effect of multimodal rehabilitation on pain, functioning, mood, active range of motion, cognitive functions. Participants will undergo a 4-week program of multimodal rehabilitation of physical therapy, education and Graded Motor Imagery. Assessment will be made at baseline and after 4 weeks. Researchers will compare the interventional arm with healthy control to see if the observed psychological results are exclusive to CRPS group. There is no expanded access scheduled for this study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Complex Regional Pain Syndromes
Keywords
CRPS, cognitive functions, physical therapy, pain, Graded Motor Imagery, mirror therapy, rehabilitation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Treatment arm will undergo a 4-week multimodal rehabilitation program with outcome measures recorded at baseline and at 4 weeks. Healthy control will be assessed for psychological outcome measures at baseline and at 4 weeks, with no intervention applied.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
42 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CRPS
Arm Type
Experimental
Arm Description
Participants meeting inclusion and exclusion criteria undergoing 4-week multimodal rehabilitation, undergoing assessment at baseline and at 4 weeks.
Arm Title
Healthy Control
Arm Type
No Intervention
Arm Description
Participants matched according to sex, age and education to experimental arm, undergoing psychological assessment at baseline and at 4 weeks.
Intervention Type
Other
Intervention Name(s)
Multimodal rehabilitation
Intervention Description
The multimodal rehabilitation program included comprehensive therapy 5 times a week during the 4 weeks between assessments. The therapy consists of: Individual physical therapy focused on improving range of motion and alleviating pain in the affected limb; Mechanical desensitization; Transcutaneous electric nerve stimulation (TENS) electrotherapy; Aquatherapy (arm or leg whirlpool bath of the affected extremity); Graded Motor Imagery, including the Recognise™ app and mirror therapy; Psychoeducation on relaxation and coping with chronic pain.
Primary Outcome Measure Information:
Title
Mean change from baseline in Reproduction score on the Rey's Complex Figure Test (RCFT) score at 4 weeks.
Description
The RCFT is a task-based test assessing visual-spatial abilities. Reproduction score measures learning and planning on visual material. Possible scores range from 0 (significant deficit) to 36 (highest possible score). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Secondary Outcome Measure Information:
Title
Mean change from baseline in Copy score on the Rey's Complex Figure Test (RCFT) score at 4 weeks.
Description
The RCFT is a task-based test assessing visual-spatial abilities. Copy score measures planning on visual material. Possible scores range from 0 (significant deficit) to 36 (highest possible score). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in pain score on the Numeric Rating Scale (NRS) at 4 weeks
Description
The NRS is a self-reported instrument assessing average pain intensity over the past 24 hour period. Possible scores range from 0 (no pain) to 10 (worst possible pain). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Disabilities of the Arm, Shoulder, and Hand Questionnaire (DASH) at 4 weeks in Participants with upper extremity CRPS
Description
The DASH is a self-reported instrument assessing ability to perform certain upper extremity activities. Possible scores range from 0 (no disability) to 100 (complete disability). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Lower Extremity Functional Scale (LEFS) at 4 weeks in Participants with lower extremity CRPS
Description
The LEFS is a self-reported instrument assessing ability to perform certain lower extremity activities. Possible scores range from 0 (complete disability) to 80 (no disability). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Number of Participants meeting the Budapest Criteria for CRPS at baseline as percent of Participants in the CRPS arm
Description
The Budapest Criteria are a set of clinical criteria used to diagnose CRPS. Possible outcomes include: CRPS-I, CRPS-II, CRPS-RSF, not meeting Budapest Criteria. Number = ((number of CRPS-I + number of CRPS-II + number of CRPS-RSF) / total Participants in CRPS arm) * 100%.
Time Frame
Baseline
Title
Mean change from baseline in active range of motion (aROM) of affected joint at 4 weeks
Description
The aROM is a clinical measure calculated as an angle between extreme positions of a joint. Possible scores range from 0° (no motion) to 360° (full rotation). Change = ((week 4 score / baseline score) * 100%).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Central Sensitization Inventory (CSI) part A at 4 weeks
Description
The CSI is a self-reported instrument assessing overlapping health-related symptom dimensions of central sensitization. Possible scores range from 0 (subclinical) to 100 (extreme). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Short-Form McGill Pain Questionnaire (SF-MPQ) part A score at 4 weeks
Description
The SF-MPQ is a self-reported instrument assessing different types of pain. Possible scores range from 0 (no pain) to 45 (severe pain). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in PainDetect Questionnaire (PDQ) score at 4 weeks
Description
The PDQ is a self-reported instrument assessing neuropathic pain. Possible scores range from -1 (neuropathic component <15%) to 38 (neuropathic component >90%). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Diverting Attention score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
Description
The CSQ is a self-reported instrument assessing different pain coping strategies. The Diverting Attention score measures the use of attention diversion as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 36 (strategy significantly engaged). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Reinterpreting Pain Sensations score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
Description
The CSQ is a self-reported instrument assessing different pain coping strategies. The Reinterpreting Pain Sensations score measures the use of pain sensation reinterpretation as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 36 (strategy significantly engaged). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Catastrophizing score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
Description
The CSQ is a self-reported instrument assessing different pain coping strategies. The Catastrophizing score measures the use of catastrophising as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 36 (strategy significantly engaged). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Ignoring Sensation score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
Description
The CSQ is a self-reported instrument assessing different pain coping strategies. The Ignoring Sensation score measures the use of ignoring pain sensation as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 36 (strategy significantly engaged). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Praying or Hoping score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
Description
The CSQ is a self-reported instrument assessing different pain coping strategies. The Praying or Hoping score measures the use of prayer and wishful thinking as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 36 (strategy significantly engaged). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Coping Self Statements score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
Description
The CSQ is a self-reported instrument assessing different pain coping strategies. The Coping Self Statements score measures positive self-affirmations as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 36 (strategy significantly engaged). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Increased Behavioral Activity score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
Description
The CSQ is a self-reported instrument assessing different pain coping strategies. The Increased Behavioral Activity score measures the use of behavioral activity increase as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 36 (strategy significantly engaged). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Control Over Pain score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
Description
The CSQ is a self-reported instrument assessing different pain coping strategies. The Control Over Pain score measures the notion of control over pain as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 6 (strategy significantly engaged). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Ability to Decrease Pain score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
Description
The CSQ is a self-reported instrument assessing different pain coping strategies. The Ability to Decrease Pain score measures the notion of being able to decrease pain as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 6 (strategy significantly engaged). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean score on the Mini-Mental State Examination (MMSE) at baseline.
Description
The MMSE is a clinician-reported screening test assessing general cognitive functioning. Possible scores range from 0 (severe cognitive deficit) to 30 (no cognitive deficit).
Time Frame
Baseline
Title
Mean change from baseline in Total Number Correct score in Benton Visual Retention Test (BVRT) at 4 weeks.
Description
The BVRT is a task-based test assessing visual-spatial working memory and visual-spatial abilities. Total Number Correct score counts correct answers. Possible scores range from 0 (significant deficit) to 10 (highest possible score). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Number of Errors score in the Benton Visual Retention Test (BVRT) at 4 weeks.
Description
The BVRT is a task-based test assessing visual-spatial working memory and visual-spatial abilities. Number of Errors score counts wrong answers. Possible scores range from 0 (best possible score) to 10 (worst possible score). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Digit Span (DS) score in Wechsler's Adult Intelligence Scale Revised (WAIS-R) at 4 weeks.
Description
WAIS-R is a task-based test assessing intelligence. The DS score measures attention and working memory. Possible scores range from 0 (significant deficit) to 28 (highest possible score). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Beck Depression Inventory - II (BDI-II) score at 4 weeks.
Description
The BDI-II is a self-reported questionnaire assessing depression severity. Possible scores range from 0 (no depression) to 66 (severe depression). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Speed of Work score in the Attention and Perceptiveness Test (TUS) - at 4 weeks.
Description
The TUS is a task-based test assessing attention. Speed of Work measures number of tasks completed in a fixed amount of time. Possible scores range from 0 (lowest possible speed) to 972 (highest possible speed). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Number of Mistakes score in the Attention and Perceptiveness Test (TUS) at 4 weeks.
Description
The TUS is a task-based test assessing attention. Number of Mistakes score measures resistance to distraction. Possible scores range from 0 (perfect score) to 972 (worst possible score). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Number of Omissions in the Attention and Perceptiveness Test (TUS) at 4 weeks.
Description
The TUS is a task-based test assessing attention. Number of Omissions score measures resistance to distraction. Possible scores range from 0 (perfect score) to 349 (worst possible score). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in execution time in the Color-Trials Test part 1 (CTT-1) at 4 weeks.
Description
The CTT-1 is a task-based test assessing psychomotor speed in time (seconds). Possible scores range from 0s (impossibly fast) to infinite time (unable to complete). Change = (week 4 time in seconds - baseline time in seconds).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in shifting attention score on the Color-Trials Test part 2 (CTT-2) at 4 weeks.
Description
The CTT-2 is a task-based test assessing shifting attention in time (seconds). Possible scores range from 0s (impossibly fast) to infinite time (unable to complete task). Change = (week 4 time in seconds - baseline time in seconds).
Time Frame
At baseline and in 4 weeks
Other Pre-specified Outcome Measures:
Title
Mean change from baseline in Emotion-oriented Coping score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
Description
The CSQ is a self-reported instrument assessing 3 targets for pain-coping. The Emotion-oriented Coping score measures the tendency to have a strong emotional response to pain as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 72 (strategy significantly engaged). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Avoidance-oriented Coping score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
Description
The CSQ is a self-reported instrument assessing 3 targets for pain-coping. The Avoidance-oriented Coping score measures the tendency to avoid the source of pain as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 72 (strategy significantly engaged). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks
Title
Mean change from baseline in Task-oriented Coping score in the Coping Strategy Questionnaire (CSQ) at 4 weeks.
Description
The CSQ is a self-reported instrument assessing 3 targets for pain-coping. The Task-oriented Coping score measures the tendency to address the source of pain as a pain-coping strategy. Possible scores range from 0 (strategy not engaged) to 108 (strategy significantly engaged). Change = (week 4 score - baseline score).
Time Frame
At baseline and in 4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Clinical diagnosis of CRPS (or equivalent); MMSE >24 points; Has signed an informed consent to the study. Exclusion Criteria: MMSE ≤24 points; Inability to perform scheduled tasks (multimodal rehabilitation program).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Beata Tarnacka, ASSC PROF
Organizational Affiliation
National Institute of Geriatrics, Rheumatology and Rehabilitation
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Adam Zalewski, MD
Organizational Affiliation
National Institute of Geriatrics, Rheumatology and Rehabilitation
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Institute of Geriatrics, Rheumatology and Rehabilitation
City
Warsaw
ZIP/Postal Code
02-637
Country
Poland

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
All of the individual participant data collected during the trial, after deidentification will be made published on Open Science Framework.
IPD Sharing Time Frame
Immediately following publication. No end date.
IPD Sharing Access Criteria
Anyone who wishes to access the data.
Citations:
PubMed Identifier
34903493
Citation
Fallico N, Padmanabhan R, Rahman S, Somma F, Spagnoli AM. A randomised placebo-controlled clinical trial on the efficacy of local lidocaine injections and oral citalopram for the treatment of complex regional pain syndrome. J Plast Reconstr Aesthet Surg. 2022 Mar;75(3):970-979. doi: 10.1016/j.bjps.2021.11.022. Epub 2021 Nov 14.
Results Reference
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PubMed Identifier
34890455
Citation
Yoo Y, Lee CS, Kim J, Jo D, Moon JY. Botulinum Toxin Type A for Lumbar Sympathetic Ganglion Block in Complex Regional Pain Syndrome: A Randomized Trial. Anesthesiology. 2022 Feb 1;136(2):314-325. doi: 10.1097/ALN.0000000000004084.
Results Reference
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PubMed Identifier
34250660
Citation
Defina S, Niedernhuber M, Shenker N, Brown CA, Bekinschtein TA. Attentional modulation of neural dynamics in tactile perception of complex regional pain syndrome patients. Eur J Neurosci. 2021 Aug;54(4):5601-5619. doi: 10.1111/ejn.15387. Epub 2021 Jul 22.
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PubMed Identifier
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Citation
Lunden LK, Jorum E. The challenge of recognizing severe pain and autonomic abnormalities for early diagnosis of CRPS. Scand J Pain. 2021 Apr 12;21(3):548-559. doi: 10.1515/sjpain-2021-0036. Print 2021 Jul 27.
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Citation
Beales D, Carolan D, Chuah-Choong J, Hammond S, O'Brien E, Boyle E, Ranelli S, Holthouse D, Mitchell T, Slater H. Exploring peoples' lived experience of complex regional pain syndrome in Australia: a qualitative study. Scand J Pain. 2021 Jan 6;21(2):393-405. doi: 10.1515/sjpain-2020-0142. Print 2021 Apr 27.
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Physical and Psychological Changes in CRPS Patients Undergoing Multimodal Rehabilitation

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