Your browser doesn't support javascript.
loading
Whole-Body Photobiomodulation Therapy for Fibromyalgia: A Feasibility Trial.
Fitzmaurice, Bethany C; Heneghan, Nicola R; Rayen, Asius T A; Grenfell, Rebecca L; Soundy, Andrew A.
Afiliação
  • Fitzmaurice BC; Department of Pain Management, Sandwell and West Birmingham NHS Trust, Birmingham B71 4HJ, UK.
  • Heneghan NR; School of Sport, Exercise and Rehabilitation Sciences, University of Birmingham, Birmingham B15 2TT, UK.
  • Rayen ATA; School of Sport, Exercise and Rehabilitation Sciences, University of Birmingham, Birmingham B15 2TT, UK.
  • Grenfell RL; Department of Pain Management, Sandwell and West Birmingham NHS Trust, Birmingham B71 4HJ, UK.
  • Soundy AA; Clinical Research Facility, Sandwell and West Birmingham NHS Trust, Birmingham B71 4HJ, UK.
Behav Sci (Basel) ; 13(9)2023 Aug 29.
Article em En | MEDLINE | ID: mdl-37753995
Effective treatment for fibromyalgia (FM) is lacking and further treatment options are needed. Photobiomodulation therapy (PBMT) represents one potential treatment option. Whilst favourable findings have been reported using localised PBMT, no investigations have established the value of whole-body PBMT for the complete set of symptom domains in FM. A single-arm feasibility study was conducted in accordance with CONSORT (Consolidated Standards of Reporting Trials) guidelines. A non-probability sampling method was used to access individuals with FM. The primary outcome measure was identified as the Revised Fibromyalgia Impact Questionnaire (FIQR). Forty-nine participants were screened and twenty-one trial participants entered the trial. Nineteen participants completed the intervention (18 whole-body PBMT sessions over approximately six weeks). Descriptive statistics and qualitative analysis was undertaken to represent feasibility outcomes. Acceptability of the trial device and processes were established. Outcome measures towards efficacy data were guided by core and peripheral OMERACT (outcomes measures in rheumatological clinical trials) domains, utilising a combination of participant-reported and performance-based outcome measures. Data for the embedded qualitative component of the trial were captured by participant-reported experience measures and audio-recorded semi-structured interviews. Positive changes were observed for FM-specific quality of life, pain, tenderness, stiffness, fatigue, sleep disturbance, anxiety, depression and cognitive impairment. Patient global assessment revealed improvements at 6 weeks, with continued effect at 24 weeks. FM-specific quality of life at 24 weeks remained improved compared with baseline scores. The findings provided evidence to support a full-scale trial and showed promise regarding potential efficacy of this novel non-invasive treatment in an FM population.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article