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"Reboot Online", online multidisciplinary pain management program (MDPP). Clinical content from an existing effective face-to-face group-based MDPP (the Reboot program) was adapted to an online format, modeling traditional Internet-delivered CBT programs for common mental disorders
Usual careContinuation of current treatments; permitted to engage in any new interventions for chronic pain management during the study period; offered the online intervention after completing follow-up assessments.

Arm Details

1. Is the program practice-based or system-based?
CPMP
Usual care
2. How many patients were randomized to this treatment arm?
CPMP
Usual care
3. Program duration (weeks)
Please report the duration of the program in weeks and include "weeks" in the text box.
CPMP
Usual care
4. Number of sessions per week
Report as X sessions/week
CPMP
Usual care
5. Was the program conducted in the inpatient or outpatient setting?
Select one.
CPMP
Usual care
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
Physical Functioning/Reconditioning Components of InterventionPsychological and Mental Health Components of Intervention
Treatment types
Treatment providers
Mode of delivery
Duration of treatment
Tailoring
Adherence
Usual care
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
Usual care
8. Additional components of the intervention
CPMP
Usual care
9. Description of care coordination/collaboration
CPMP
Usual care

Sample Characteristics

N/A

Outcomes

TypeDomainSpecific measurement (i.e., tool/definition/specific outcome)PopulationsTimepoints
ContinuousPainBrief Pain Inventory Severity
  • All Participants
  • Baseline
  • Immediately post-treatment
  • 3 months
ContinuousPainBrief Pain Inventory Interference
  • All Participants
  • Baseline
  • Immediately post-treatment
  • 3 months
ContinuousPain Brief Pain Inventory
  • All Participants
  • Baseline
  • Immediately post-treatment
  • 3 months
CategoricalOpioid useOpioid use
  • All Participants
  • Baseline
  • Immediately post-treatment
  • 3 months
ContinuousDepressionPatient Health Questionnaire–9 Depression
  • All Participants
  • Baseline
  • Immediately Post-intervention
  • 3 months
ContinuousMental healthKessler-10 Psychological Distress Scale
  • All Participants
  • Baseline
  • Immediately Post-intervention
  • 3 months
ContinuousOtherPain Self-Efficacy Questionnaire
  • All Participants
  • Baseline
  • Immediately Post-intervention
  • 3 months

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


Opioid use (Opioid use)

All Participants
Descriptive StatisticsBetween Arm Comparisons
CPMPUsual care
Baseline
Total (N analyzed)
Odds Ratio (OR)
Events
95% CI low (OR)
Percentage
95% CI high (OR)
p value
Immediately post-treatment
Total (N analyzed)
Odds Ratio (OR)
Events
95% CI low (OR)
Percentage
95% CI high (OR)
p value
3 months
Total (N analyzed)
Odds Ratio (OR)
Events
95% CI low (OR)
Percentage
95% CI high (OR)
p value
Within Arm ComparisonsNet Comparisons
CPMPUsual care

Continuous


Pain (Brief Pain Inventory Severity)

All Participants
Descriptive StatisticsBetween Arm Comparisons
CPMPUsual care
Baseline
Mean
Mean Difference (MD)
SD
95% CI low (MD)
95% CI high (MD)
SD (MD)
p value (MD)
Immediately post-treatment
Mean
Mean Difference (MD)
SD
95% CI low (MD)
95% CI high (MD)
SD (MD)
p value (MD)
3 months
Mean
Mean Difference (MD)
SD
95% CI low (MD)
95% CI high (MD)
SD (MD)
p value (MD)
Within Arm ComparisonsNet Comparisons
CPMPUsual care

Pain (Brief Pain Inventory Interference)

All Participants
Descriptive StatisticsBetween Arm Comparisons
CPMPUsual care
Baseline
Mean
Mean Difference (MD)
SD
95% CI low (MD)
95% CI high (MD)
SD (MD)
p value (MD)
Immediately post-treatment
Mean
Mean Difference (MD)
SD
95% CI low (MD)
95% CI high (MD)
SD (MD)
p value (MD)
3 months
Mean
Mean Difference (MD)
SD
95% CI low (MD)
95% CI high (MD)
SD (MD)
p value (MD)
Within Arm ComparisonsNet Comparisons
CPMPUsual care

Pain (Brief Pain Inventory)

All Participants
Descriptive StatisticsBetween Arm Comparisons
CPMPUsual care
Baseline
Mean
Mean Difference (MD)
SD
95% CI low (MD)
95% CI high (MD)
SD (MD)
p value (MD)
Immediately post-treatment
Mean
Mean Difference (MD)
SD
95% CI low (MD)
95% CI high (MD)
SD (MD)
p value (MD)
3 months
Mean
Mean Difference (MD)
SD
95% CI low (MD)
95% CI high (MD)
SD (MD)
p value (MD)
Within Arm ComparisonsNet Comparisons
CPMPUsual care

Depression (Patient Health Questionnaire–9 Depression)

All Participants
Descriptive StatisticsBetween Arm Comparisons
CPMPUsual care
Baseline
Mean
Mean Difference (MD)
SD
95% CI low (MD)
95% CI high (MD)
SD (MD)
p value (MD)
Immediately Post-intervention
Mean
Mean Difference (MD)
SD
95% CI low (MD)
95% CI high (MD)
SD (MD)
p value (MD)
3 months
Mean
Mean Difference (MD)
SD
95% CI low (MD)
95% CI high (MD)
SD (MD)
p value (MD)
Within Arm ComparisonsNet Comparisons
CPMPUsual care

Mental health (Kessler-10 Psychological Distress Scale)

All Participants
Descriptive StatisticsBetween Arm Comparisons
CPMPUsual care
Baseline
Mean
Mean Difference (MD)
SD
95% CI low (MD)
95% CI high (MD)
SD (MD)
p value (MD)
Immediately Post-intervention
Mean
Mean Difference (MD)
SD
95% CI low (MD)
95% CI high (MD)
SD (MD)
p value (MD)
3 months
Mean
Mean Difference (MD)
SD
95% CI low (MD)
95% CI high (MD)
SD (MD)
p value (MD)
Within Arm ComparisonsNet Comparisons
CPMPUsual care

Other (Pain Self-Efficacy Questionnaire)

All Participants
Descriptive StatisticsBetween Arm Comparisons
CPMPUsual care
Baseline
Mean
Mean Difference (MD)
SD
95% CI low (MD)
95% CI high (MD)
SD (MD)
p value (MD)
Immediately Post-intervention
Mean
Mean Difference (MD)
SD
95% CI low (MD)
95% CI high (MD)
SD (MD)
p value (MD)
3 months
Mean
Mean Difference (MD)
SD
95% CI low (MD)
95% CI high (MD)
SD (MD)
p value (MD)
Within Arm ComparisonsNet Comparisons
CPMPUsual care