A Pilot Randomized Controlled Trial of a Guided Self-Help Intervention to Manage Chronic Orofacial Pain

被引:8
|
作者
Goldthorpe, Joanna [1 ]
Lovell, Karina [2 ]
Peters, Sarah [3 ]
McGowan, Linda [4 ]
Nemeth, Imola [5 ]
Roberts, Christopher [6 ]
Aggarwal, Vishal R. [7 ]
机构
[1] Univ Manchester, Sch Dent, Manchester, Lancs, England
[2] Univ Manchester, Sch Nursing Midwifery & Social Work, Mental Hlth, Manchester, Lancs, England
[3] Univ Manchester, Sch Psychol Sci, Psychol, Manchester, Lancs, England
[4] Univ Leeds, Appl Hlth Res, Sch Healthcare, Fac Med & Hlth, Leeds, W Yorkshire, England
[5] Univ Manchester, Unit Biostat, Sch Med, Manchester, Lancs, England
[6] Univ Manchester, Unit Biostat, Sch Med, Biostat, Manchester, Lancs, England
[7] Univ Leeds, Sch Dent, Fac Med & Hlth, Leeds LS2 9JT, W Yorkshire, England
基金
美国国家卫生研究院;
关键词
behavioral; chronic orofacial pain; pilot trial; self-help intervention; MEDICALLY UNEXPLAINED SYMPTOMS; HEALTH SURVEY QUESTIONNAIRE; COMPLEX INTERVENTIONS; CLINICAL-TRIALS; VALIDATION; FRAMEWORK; DISORDER; RISK;
D O I
10.11607/ofph.1665
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Aims: To conduct a pilot trial to test the feasibility of a guided self-help intervention for chronic orofacial pain. Methods: A pilot randomized controlled trial was conducted to compare the intervention with usual treatment. A total of 37 patients with chronic orofacial pain were randomized into either the intervention group (n = 19) or the usual treatment (control) group (n = 18). Validated outcome measures were used to measure the potential effectiveness of the intervention over a number of domains: physical and mental functioning (Short Form 36 [SF-36]); anxiety and depression (Hospital Anxiety and Depression Scale [HADS]); pain intensity and interference with life (Brief Pain Inventory [BPI]); disability (Manchester Orofacial Pain Disability Scale [MOPDS]); and illness behavior (Revised Illness Perceptions Questionnaire [IPQr]). Bootstrap confidence intervals were computed for the treatment effect (ES) posttreatment and at 3 months follow-up and adjusted for baseline values of the outcome measure by using analysis of covariance. Results: At posttreatment and the 3-month follow-up, 11 participants in the intervention group and 7 in the control group failed to complete outcome measures. The intervention was acceptable and could be feasibly delivered face to face or over the telephone. Although the pilot trial was not powered to draw conclusions about the effectiveness, it showed significant (P <.05) effects of the intervention on physical and mental functioning and treatment control. Conclusion: The self-help intervention was acceptable to patients and allowed them to better understand and self-manage chronic orofacial pain. It showed potential effectiveness on outcome domains related to functioning and illness perception. Further research is needed to understand the cost effectiveness of the intervention for chronic orofacial pain.
引用
收藏
页码:61 / 71
页数:11
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