ArticlePain medicine (Malden, Mass.)2026
Acceptance and commitment therapy for prevention of chronic pain after total knee arthroplasty.
Article in Pain medicine (Malden, Mass.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05769998 (Development and Improvement of an Acceptance and Commitment-based Treatment for the Prevention of Chronic Pain After Total Knee Arthroplasty), which is not on this map. Cited by 1 paper.
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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.
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.
Development and Improvement of an Acceptance and Commitment-based Treatment for the Prevention of Chronic Pain After Total Knee Arthroplasty
Who cites it
1 citing paper in PubMed.
- Coping to move again: the psychological dimension of tele-supported rehabilitation after knee arthroplasty-A randomized controlled trial.Frontiers in digital health · 2026Article
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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
Abstract
objectiveThe aims of this study are to assess the preliminary outcomes of the NOPAIN treatment, which is an acceptance and commitment therapy-based treatment performed in the early postoperative period after total knee arthroplasty (TKA), aimed to prevent the onset of chronic postsurgical pain, as well as to evaluate the predictors of the presence of moderate-to-severe pain after 3 months.
designNon-controlled preliminary trial.
settingDivision of Rehabilitation Medicine within an Italian tertiary care hospital. SUBJECTS: Eighty patients undergoing postoperative rehabilitation after TKA.
methodsBefore the treatment, patients underwent a baseline assessment of pain intensity (Numeric Rating Scale), knee pain, stiffness and function (WOMAC), as well as of potential predictors of the effects of the treatment, namely sex, age, pain duration, catastrophizing (Pain Catastrophizing Scale), psychological distress (Hospital Anxiety and Depression Scale), presence of central sensitization (Central Sensitization Inventory), cognitive flexibility (Wisconsin Card Sorting Test), and heart rate variability. Then, all patients underwent the NOPAIN treatment. Pain intensity, knee pain, stiffness and function, catastrophizing, and psychological distress were also assessed after 3 months.
resultsParticipation rate was 72% and retention was high, with 81.3% of participants completing all 4 sessions of the NOPAIN treatment. Pain intensity (P < .01), knee pain (P < .01), knee stiffness (P < .01), and knee function (P < .01) improved over time. Female sex and age were associated with lower odds of moderate-to-severe pain at 3 months, whereas presence of central sensitization, baseline pain intensity, rumination, helplessness, and changes in helplessness were associated with higher odds.
conclusionThis study shows that the NOPAIN treatment is feasible, that it can be integrated into standard rehabilitative care, and that it might contribute to the prevention of chronic post-surgical pain. The results of this preliminary study will be the basis for the improvement of the intervention. CLINICAL TRIALS REGISTRATION: This preliminary trial is part of a broader research project registered in ClinicalTrials.gov (registration number: NCT05769998, link: https://clinicaltrials.gov/study/NCT05769998). Patient enrolment started on June 15, 2021.
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