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Joint mobilization vs massage for chronic mechanical neck pain: a pilot study to assess recruitment strategies and estimate outcome measure variability.

Journal of manipulative and physiological therapeutics
January 1, 2010
Timothy J Madson et al. (3 authors)
Journal ArticleRandomized Controlled TrialHuman StudyClinical
Study Details

Study Goal

The researchers aimed to assess the feasibility of a trial comparing cervical spine mobilization and massage as adjuncts to usual physical therapy for chronic neck pain, including recruitment strategies and variability in outcomes.

Results Summary

The study found that massage, alongside postural education and home exercises, resulted in improved Neck Disability Index (NDI) and pain VAS scores, though the effect was modest. Recruitment challenges were noted, requiring strategy adjustments for future trials.

Population

Adults with nonspecific chronic neck pain (≥3 months).

Effective Dosage

Not specified (12 treatments total).

Duration

Duration of individual treatments not specified; total intervention involved 12 sessions.

Interactions

None mentioned.

Extracted Claims (4)
InterventionDirectionEndpointPopulationDosageImpactClaim #
cervical spine joint mobilization
decrease
Neck Disability Index (NDI) score
subjects with chronic nonspecific neck pain
from 13.54 to 5.64
reduced
#1
cervical spine joint mobilization
decrease
pain VAS score
subjects with chronic nonspecific neck pain
from 40.91 to 16.54
reduced
#2
sedative massage
decrease
Neck Disability Index (NDI) score
subjects with chronic nonspecific neck pain
from 12.75 to 8.08
reduced
#3
sedative massage
decrease
pain VAS score
subjects with chronic nonspecific neck pain
from 29.42 to 20.91
reduced
#4
Abstract

OBJECTIVE: The purpose of this study was to determine the feasibility of a trial comparing cervical spine mobilization and massage as adjuncts to usual physical therapy treatments (superficial heat and head and neck posture education) for chronic neck pain. Specific objectives were to assess procedures and recruitment strategies and estimate the variability of the Neck Disability Index (NDI) and visual analog scale (VAS) in a population of subjects with chronic nonspecific neck pain and calculate a sample size for a definitive trial. METHODS: Subjects with nonspecific chronic neck pain (≥3 months) were randomized to receive either sedative massage or cervical spine joint mobilization in addition to postural education and home exercises. Neck Disability Index (primary outcome) and pain VAS scores were recorded for pretreatment, posttreatment, and change scores within each group to estimate effect size. Recruitment and follow-up success rates were tracked. RESULTS: Sixty potential subjects were screened: 34 were eligible and 23 were enrolled. The primary reason for not participating was the unwillingness to commit to the treatment schedule. Twenty subjects completed all (12) treatments. Three subjects discontinued treatment because they become asymptomatic. Pre and post mean NDI and VAS scores for the group receiving joint mobilization were 13.54/5.64 and 40.91/16.54, respectively. Pre and post mean NDI and VAS for the group receiving massage were 12.75/8.08 and 29.42/20.91, respectively. Several problems were encountered, and possible solutions were identified. Recruitment difficulties required alteration of the recruitment strategy. CONCLUSION: A full scale trial is feasible if appropriate changes are made in recruitment strategy including recruiting from a wider referral base, direct recruitment from the community, and/or expanding the study to multiple sites. A clinical trial will require 66 subjects per group to have a power of 80% to detect a 2-point difference in NDI score. This sample size will also provide more than 80% power to detect a 10-point difference in pain (VAS) between groups. Recruitment goals will be 76 per group to allow for dropouts.

Medical Subject Headings (MeSH)
Chronic DiseaseDisability EvaluationExercise TherapyFemaleHumansMaleManipulation, OrthopedicMassageMiddle AgedNeck PainPain MeasurementPatient SelectionPilot ProjectsPostureRandomized Controlled Trials as Topic
Study Links
Quality Scores
SafetyNot Assessed
Efficacy65/10
Quality75/10
Citation Metrics
Total Citations21
Citations/Year1.4
Relative Citation Ratio0.95
NIH Percentile48.3%
Research Impact Scores
APT Score0.50
Weight Score1.20
Normalized Score0.61
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