Extraction form for project: IPMP (Integrated Pain Management Programs)

Design Details

1. What type of program does the study assess (IPMP or CPMP)?
Integrated Pain Management Program (IPMP): Based in, integrated with, coordinated by primary care. Comprehensive Pain Management Program (CPMP): Referral based and separate from primary care.
2. In what country was the study conducted?
List all applicable countries.
3. What study design was used?
Please select the appropriate study design for the study. If the study design is not listed, you may add the appropriate study design.
4. Mean age
Report across all patients included in relevant study arms. Round to whole number. Include the word "years" after reporting the mean age.
5. % male
Report across all patients included in relevant study arms. Round to whole number. Include "%" symbol.
6. % Non-white
Report across all patients included in relevant study arms. Round to whole number. Include "%" symbol. If not reported, put NR.
7. Mean duration of pain or symptoms
Report across all patients included in relevant study arms. Round to whole number. Report duration in terms of months. If not reported, put NR.
8. Pain etiology/type
9. Disability
Disability can be measured in several ways. For example, authors may report the percent of patients receiving disability payments or they may report the mean score of a continuous disability scale such as the Pain Disability Index. Either are appropriate here, just be explicit about what is being reported.
10. Comorbidities
Extract the percent of patients with relevant comorbidities. Round percentages to whole numbers. If not reported, put NR.
% Depression diagnosis
% Anxiety diagnosis
% PTSD disagnosis
% Overweight or obese
% w/ Substance Use Disorder
% Smokers
% Suicidal
11. Randomized, Analyzed, and Attrition (at longest followup point)
For attrition report as: % (n/N)
Randomized
Analyzed
Attrition
12. How was the study funded?
13. Notes and comments

Arms

Arm NameArm Description
CPMP - Higher hoursHigh intensity outpatient interdisciplinary pain rehabilitation program
CPMP - Lower hoursLow intensity outpatient interdisciplinary pain rehabilitation

Arm Details

1. Is the program practice-based or system-based?
CPMP - Higher hours
CPMP - Lower hours
2. How many patients were randomized to this treatment arm?
CPMP - Higher hours
CPMP - Lower hours
3. Program duration (weeks)
Please report the duration of the program in weeks and include "weeks" in the text box.
CPMP - Higher hours
CPMP - Lower hours
4. Number of sessions per week
Report as X sessions/week
CPMP - Higher hours
CPMP - Lower hours
5. Was the program conducted in the inpatient or outpatient setting?
Select one.
CPMP - Higher hours
CPMP - Lower hours
6. Physical Functioning/Reconditioning & Psychological and Mental Health Components of Intervention
For treatment providers, you may write-in any options that are needed that are not already presented. For duration of treatment report as "X sessions per week over X weeks", when possible. For anything not reported, put NR.
CPMP - Higher hours
Physical Functioning/Reconditioning Components of InterventionPsychological and Mental Health Components of Intervention
Treatment types
Treatment providers
Mode of delivery
Duration of treatment
Tailoring
Adherence
CPMP - Lower hours
Physical Functioning/Reconditioning Components of InterventionPsychological and Mental Health Components of Intervention
Treatment types
Treatment providers
Mode of delivery
Duration of treatment
Tailoring
Adherence
7. Medication Review and/or Management Components of Intervention
CPMP - Higher hours
CPMP - Lower hours
8. Additional components of the intervention
CPMP - Higher hours
CPMP - Lower hours
9. Description of care coordination/collaboration
CPMP - Higher hours
CPMP - Lower hours

Sample Characteristics

N/A

Outcomes

TypeDomainSpecific measurement (i.e., tool/definition/specific outcome)PopulationsTimepoints
ContinuousPainPain Disability Index
  • All Participants
  • Baseline
  • Post-treatment
ContinuousPainEuroqol 5D VAS
  • All Participants
  • Baseline
  • Post-treatment
ContinuousQOLEuroqol 5D Index
  • All Participants
  • Baseline
  • Post-treatment
CategoricalAdverse eventsAdverse events
  • All Participants
  • Baseline

Outcome Details

N/A

Risk of Bias Assessment

1. Randomization adequate?
Rating
2. Allocation concealment adequate?
Rating
3. Groups similar at baseline?
Rating
4. Outcome assessors masked?
Rating
5. Care providers masked?
Rating
6. Patient masked?
Rating
7. Reporting of attrition, crossovers, adherence, and contamination?
Rating
8. Loss to followup acceptable?
Overall ≤20%?
Difference between groups <10%?
9. Intention-to-treat (ITT) analysis?
Overall ≤20%?
10. Outcomes prespecified?
Overall ≤20%?
11. Quality determination
Overall ≤20%?

Results

Categorical


Adverse events (Adverse events)

All Participants
Descriptive StatisticsBetween Arm Comparisons
CPMP - Higher hoursCPMP - Lower hours
Baseline
Total (N analyzed)
Odds Ratio (OR)
Note
95% CI low (OR)
95% CI high (OR)
p value
Within Arm ComparisonsNet Comparisons
CPMP - Higher hoursCPMP - Lower hours

Continuous


Pain (Pain Disability Index)

All Participants
Descriptive StatisticsBetween Arm Comparisons
CPMP - Higher hoursCPMP - Lower hours
Baseline
Total (N analyzed)
Mean Difference (MD)
Mean
95% CI low (MD)
SD
95% CI high (MD)
SD
SD (MD)
p value (MD)
Post-treatment
Total (N analyzed)
Mean Difference (MD)
Mean
95% CI low (MD)
SD
95% CI high (MD)
SD
SD (MD)
p value (MD)
Within Arm ComparisonsNet Comparisons
CPMP - Higher hoursCPMP - Lower hours

Pain (Euroqol 5D VAS)

All Participants
Descriptive StatisticsBetween Arm Comparisons
CPMP - Higher hoursCPMP - Lower hours
Baseline
Total (N analyzed)
Mean Difference (MD)
Mean
95% CI low (MD)
SD
95% CI high (MD)
SD
SD (MD)
p value (MD)
Post-treatment
Total (N analyzed)
Mean Difference (MD)
Mean
95% CI low (MD)
SD
95% CI high (MD)
SD
SD (MD)
p value (MD)
Within Arm ComparisonsNet Comparisons
CPMP - Higher hoursCPMP - Lower hours

QOL (Euroqol 5D Index)

All Participants
Descriptive StatisticsBetween Arm Comparisons
CPMP - Higher hoursCPMP - Lower hours
Baseline
Total (N analyzed)
Mean Difference (MD)
Mean
95% CI low (MD)
SD
95% CI high (MD)
SD
SD (MD)
p value (MD)
Post-treatment
Total (N analyzed)
Mean Difference (MD)
Mean
95% CI low (MD)
SD
95% CI high (MD)
SD
SD (MD)
p value (MD)
Within Arm ComparisonsNet Comparisons
CPMP - Higher hoursCPMP - Lower hours