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.
Single Choice
IPMP
CPMP
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.
Single Choice
RCT
Cluster RCT
Prospective comparative cohort
Retrospective comparative cohort
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
Single Choice
Chronic low back pain
Fibromyalgia
Mixed or multiple chronic pain conditions
Rheumatic disease
Chronic nonspecific spinal pain
Acute low back pain
Traumatic injury
Osteoarthritis
Subacute low back pain
Chronic musculoskeletal pain
Chronic widespread pain
Chronic musculoskeletal pain or neuropathic pain
Multiple sources (patient could have more than one pain type, including: back, head, arm, leg, chest, and abdomen)
Back pain
Back and neck pain
Head, neck, shoulders, arms, back, and/or legs
Low back and/or leg pain
Dorsalgia, arthrosis, and/or other dorsopathies, not otherwise classified,
Cervical, arm, head, knee, lumbar, leg, shoulder, whole back, widespread areas, and/or radiating pain
Lumbar disk hernia
Low back pain
Injury related pain (51%), Non-injury related pain (49%)
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

Arm Details

1. Is the program practice-based or system-based?
2. How many patients were randomized to this treatment arm?
3. Program duration (weeks)
Please report the duration of the program in weeks and include "weeks" in the text box.
4. Number of sessions per week
Report as X sessions/week
5. Was the program conducted in the inpatient or outpatient setting?
Select one.
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.
7. Medication Review and/or Management Components of Intervention
8. Additional components of the intervention
9. Description of care coordination/collaboration

Sample Characteristics

N/A

Outcome Details

N/A

Risk of Bias Assessment

1. Randomization adequate?
Rating
Single Choice
Yes
No
Unclear
2. Allocation concealment adequate?
Rating
Single Choice
Yes
No
Unclear
3. Groups similar at baseline?
Rating
Single Choice
Yes
No
Unclear
4. Outcome assessors masked?
Rating
Single Choice
Yes
No
Unclear
5. Care providers masked?
Rating
Single Choice
Yes
No
Unclear
6. Patient masked?
Rating
Single Choice
Yes
No
Unclear
7. Reporting of attrition, crossovers, adherence, and contamination?
Rating
Single Choice
Yes
No
Unclear
8. Loss to followup acceptable?
Overall ≤20%?
Single Choice
Yes
No
Unclear
Difference between groups <10%?
Single Choice
Yes
No
Unclear
9. Intention-to-treat (ITT) analysis?
Overall ≤20%?
Single Choice
Yes
No
Unclear
10. Outcomes prespecified?
Overall ≤20%?
Single Choice
Yes
No
Unclear
11. Quality determination
Overall ≤20%?
Single Choice
Poor
Fair
Good

Suggested Arms

NameDescription
Total All arms combined

Please see downloadable data for more

Suggested Outcomes

N/A