Evidence map›Paper›PMID 22313547›Full record

Trial reportPain medicine (Malden, Mass.)2012

Addressing both depression and pain in late life: the methodology of the ADAPT study.

Jordan F Karp, Bruce L Rollman, Charles F Reynolds, Jennifer Q Morse, Frank Lotrich, Sati Mazumdar, Natalia Morone, Debra K Weiner

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Pain medicine (Malden, Mass.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
2.2field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Chronic Pain and Opioids in the Elderly: Treating the Brain, Not Just the Body.International journal of environmental research and public health · 2026
    Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Problem-Solving Therapy in the Elderly.Current treatment options in psychiatry · 2014
    Article
  13. Article
  14. Risk factors for restricting back pain in older persons.Journal of the American Medical Directors Association · 2014
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Jordan F KarpDepartments of Psychiatry, University of Pittsburgh and University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA. karpjf@upmc.edu
Bruce L Rollman
Charles F Reynolds
Jennifer Q Morse
Frank Lotrich
Sati Mazumdar
Natalia Morone
Debra K Weiner
University of Pittsburgh · US

Funding

VARIABILITY, STABILITY & SMOOTHNESS OF WALKINGP30AG024827 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JENNIFER S BRACH · 2004 to 2026
$28.6M
University of Pittsburgh Clinical and Translational Science InstitutionKL2RR024154 · NCRR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2006 to 2011
$22.2M
University of Pittsburgh Clinical and Translational Science InstitutionKL2TR000146 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2012 to 2015
$8.7M
Optimizing Care for Older Adults with Back Pain and DepressionR01AG033575 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KARP, JORDAN F · 2010 to 2014
$2.3M
NCATS NIH HHS KL2 TR000146NCRR NIH HHS KL2 RR024154NIA NIH HHS AG033575NIA NIH HHS P30 AG024827NIA NIH HHS R01 AG033575
6 · The paper itself

Abstract

objectiveTo describe the methodology of the first NIH-funded clinical trial for seniors with comorbid depression and chronic low back pain.

methodsRandomized controlled effectiveness trial using stepped care methodology. Participants are ≥60 years old. Phase 1 (6 weeks) is open treatment with venlafaxine xr 150 mg/day and supportive management (SM). Response is 2 weeks of PHQ-9 ≤5 and at least 30% improvement in the average numeric rating scale for pain. Nonresponders progress to phase 2 (14 weeks) in which they are randomized to high-dose venlafaxine xr (up to 300 mg/day) with problem solving therapy for depression and pain (PST-DP) or high-dose venlafaxine xr and continued SM. Primary outcomes are the univariate pain and depression response and both observed and self-reported disability. Survival analytic techniques will be used, and the clinical effect size will be estimated with the number needed to treat. We hypothesize that self-efficacy for pain management will mediate response for subjects randomized to venlafaxine xr and PST-DP.

resultsNot applicable.

conclusionsThe results of this trial will inform the care of these complex patients and further understanding of comorbid pain and depression in late life.

Indexed as

AdultAgedAntidepressive Agents, Second-GenerationBehavior TherapyComorbidityCyclohexanolsDepressionFemaleHumansLow Back PainMaleMiddle AgedProblem SolvingResearch DesignVenlafaxine HydrochlorideAntidepressive Agents, Second-GenerationCyclohexanolsVenlafaxine Hydrochloride

Identifiers

PMID22313547
PMCPMC3309151
OpenAlexW1564796728

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.