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1.
Pediatrics ; 153(2)2024 Jan 01.
Artigo em Inglês | MEDLINE | ID: mdl-38282541

RESUMO

BACKGROUND: Pediatric obesity rates in the United States remain at an all-time high. Pediatric primary care clinicians and registered dietitians can help treat childhood obesity, and motivational interviewing (MI) has shown promising effects in prior trials. METHODS: We randomized 18 pediatric primary care practices to receive the Brief Motivational Interviewing to Reduce BMI or BMI2+ intervention or continue with usual care (UC). Practices were recruited through the American Academy of Pediatrics Pediatric Research in Office Settings network. The intervention comprised 4 components1: in-person and telehealth MI counseling by pediatric clinicians; 4 recommended sessions,2 6 telephone MI counseling sessions from a registered dietitian,3 text message reminders and tailored motivational messages, and4 parent educational materials. The main outcome was the change in the percentage of the 95th percentile of BMI. The study was conducted 2017 through 2021. RESULTS: There was a significant treatment x time interaction (b = 0.017, 95% confidence interval: [0.0066-0.027]) for the main outcome, favoring the UC group, with youth in the intervention arm showing a greater relative increase in their percent of the 95th percentile. CONCLUSIONS: There was no overall benefit of the intervention and, contrary to expectations, youth in the intervention arm gained more weight, based on percent of the distance from the 95th percentile than matched youth from UC practices. The absolute excess weight gain among intervention relative to UC youth was small, approximately 0.5 BMI units and 1 kg over 2 years. We offer several potential explanations for these unexpected findings.


Assuntos
Entrevista Motivacional , Obesidade Infantil , Adolescente , Criança , Humanos , Índice de Massa Corporal , Aconselhamento , Obesidade Infantil/prevenção & controle , Obesidade Infantil/psicologia , Atenção Primária à Saúde
2.
BMJ Open ; 10(7): e035720, 2020 07 28.
Artigo em Inglês | MEDLINE | ID: mdl-32723736

RESUMO

INTRODUCTION: Primary care remains an underused venue for prevention and management of paediatric overweight and obesity. A prior trial demonstrated a significant impact of paediatrician/nurse practitioner (Ped/NP)-and registered dietitian (RD)-delivered motivational interviewing (MI) on child body mass index (BMI). The study described here will test the effectiveness of an enhanced version of this primary care-based MI counselling intervention on child BMI. METHODS AND ANALYSIS: This cluster randomised effectiveness trial includes 24 Ped/NPs from 18 paediatric primary care practices that belong to the American Academy of Pediatrics (AAP) national Pediatric Research in Office Settings (PROS) practice-based research network. To date, practices have been randomised (nine to intervention and nine to usual care). Intervention Ped/NPs have been trained in MI, behavioural therapy, billing/coding for weight management and study procedures. Usual care Ped/NPs received training in billing/coding and study procedures only. Children 3- 11 years old with BMI >the 85th percentile were identified via electronic health records (EHRs). Parents from intervention practices have been recruited and enrolled. Over about 2 years, these parents are offered approximately 10 MI-based counselling sessions (about four in person sessions with their child's Ped/NP and up to six telephonic sessions with a trained RD). The primary outcome is change in child BMI (defined as per cent from median BMI for age and sex) over the study period. The primary comparison is between eligible children in intervention practices whose parents enrol in the study and all eligible children in usual care practices. Data sources will include EHRs, billing records, surveys and counselling call notes. ETHICS AND DISSEMINATION: Institutional Review Board approval was obtained from the AAP. All Ped/NPs provided written informed consent, and intervention group parents provided consent and Health Insurance Portability and Accountability Act (HIPAA) authorisation. Findings will be disseminated through peer-reviewed publications, conference presentations and appropriate AAP channels. TRIAL REGISTRATION NUMBER: NCT03177148; Pre-results.


Assuntos
Protocolos Clínicos , Entrevista Motivacional/normas , Obesidade/terapia , Sobrepeso/terapia , Índice de Massa Corporal , Criança , Pré-Escolar , Feminino , Humanos , Masculino , Entrevista Motivacional/métodos , Obesidade/psicologia , Sobrepeso/psicologia , Pediatria/métodos , Atenção Primária à Saúde/métodos
3.
Spine (Phila Pa 1976) ; 28(13): 1435-46, 2003 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-12838103

RESUMO

STUDY DESIGN: A two-part investigation was conducted: 1) a prospective study of asymptomatic subjects quantitatively comparing trunk mobility to surface electromyographic (sEMG) signals from the erector spinae during trunk flexion; and 2) a prospective repeated-measures cohort study of patients with chronic disabled work-related spinal disorder tested for the flexion-relaxation (FR) phenomenon while measured simultaneously for lumbar spine inclinometric range of motion (ROM). OBJECTIVES: To describe a theoretical model for the potential use of FR unloaded in assessing patients with chronic low back pain patients before and after rehabilitation, and to establish a normative database (Part 1) for subsequent use in comparison to patients with chronic low back pain (Part 2). The second part of the study assessed the clinical utility of combined sEMG and ROM measurements for assessing the FR phenomenon as a test to assist potentially in planning rehabilitation programs, guiding patients' individual rehabilitation progress, and identifying early posttreatment outcome failures. SUMMARY OF BACKGROUND DATA: The FR phenomenon has been recognized since 1951, and it can be reproducibly assessed in normal subjects with FR unloaded. It can be found intermittently in patients with chronic low back pain. Recent studies have moved toward deriving formulas to identify FR, but only a few have examined a potential relation between inclinometric lumbar motion measures and the sEMG signal. No previous studies have developed normative data potentially useful for objectively assessing nonoperative treatment progress, effort, or the validity of permanent impairment rating measures. METHODS: In Part 1, 12 asymptomatic subjects were evaluated in an intra- and interrater repeated-measures protocol to examine reliability of sEMG signal readings in FR, as well as ROM measures at FR and maximum voluntary flexion. The mean sEMG signal averaging right-left electrode recordings, as well as the gross, true, and sacral lumbar ROM measurements, were recorded as normative data. In Part 2, 54 patients with chronic disabled work-related spinal disorder referred as candidates for tertiary functional restoration rehabilitation participated in a standardized assessment protocol for sEMG and ROM measurement before rehabilitation. Those who completed the program were retested with the identical methodology after rehabilitation (n = 34) using the empirically derived cutoff scores for sEMG readings at FR and ROM from Part 1 and prior scientific literature. Pain disability self-reported scores were correlated with sEMG and ROM. Sensitivity and specificity of the sEMG for identifying abnormal motion were assessed. RESULTS: In Part 1, the ability of the experienced testers to measure ROM and sEMG reliably at FR was high (r >or= 0.92; P < 0.001). All asymptomatic subjects achieved FR at a tightly clustered range of mean sEMG signals from 1 to 2.3 microV. Most of the variation between motion at FR and maximum voluntary flexion occurred through the hip (sacral) motion component of the gross (or total) motion measured at T12. In Part 2, posttreatment reliability for ROM, sEMG, and the ability to detect the FR point was high (r >or= 0.82; P < 0.001). More than 30% of the 54 patients tested before treatment demonstrated ability to achieve FR, with FR usually associated with higher ROM than in the non-FR patients. After treatment, 94% of those who completed the program achieved FR, including all those who achieved FR before treatment. Flexion-relaxation was associated with major improvement in ROM and pain disability self-report. CONCLUSIONS: Flexion-relaxation measures a point at which true lumbar flexion ROM approaches its maximum in asymptomatic subjects. This also is the point at which lumbar extensor muscle contraction relaxes, allowing the lumbar spine to hang on its posterior ligaments. The gluteal and hamstring muscles then lower the flexed trunk even further by allowing the pelvis to rotate around the hips. This phenomenon was subsequently found in Part 2 to offer a potentially promising method for individualizing rehabilitation treatment, decreasing unnecessary utilization, identifying potential postrehabilitation treatment failures, and assessing permanent impairment rating validity. Moreover, this is the first study to demonstrate systematically that an absence of FR in patients with chronic low back pain can be corrected with treatment.


Assuntos
Eletromiografia/estatística & dados numéricos , Contração Muscular , Músculo Esquelético/fisiopatologia , Doenças Profissionais/fisiopatologia , Amplitude de Movimento Articular/fisiologia , Doenças da Coluna Vertebral/fisiopatologia , Abdome/fisiologia , Adulto , Dorso/fisiologia , Estudos de Coortes , Eletromiografia/métodos , Feminino , Humanos , Região Lombossacral , Masculino , Contração Muscular/fisiologia , Músculo Esquelético/fisiologia , Variações Dependentes do Observador , Doenças Profissionais/diagnóstico , Doenças Profissionais/reabilitação , Valor Preditivo dos Testes , Estudos Prospectivos , Valores de Referência , Reprodutibilidade dos Testes , Sensibilidade e Especificidade , Doenças da Coluna Vertebral/diagnóstico , Doenças da Coluna Vertebral/reabilitação , Coluna Vertebral/fisiologia , Tórax/fisiologia
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