Research Article

A Randomized Clinical Hypnosis Pilot Study: Improvements in Self-Reported Pain Impact in Adults with Sickle Cell Disease

Table 5

Baseline clinical data and clinically relevant lab values (n = 31).

TotalGroup A (n = 15)Group B (n = 15)

Clinically relevant lab valuesMean (SD)
min–max
Mean (SD)Mean (SD)
Fetal hemoglobin12.1 (±7.3)
0.0–27.4
14.2 (±8.4)10.1 (±5.6)
Red blood cell count2.7 (±0.5)
1.76–3.82
2.7 (±0.5)2.6 (±0.6)
Hematocrit26.7 (±3.5)
19.3–34.2
27.2 (±2.4)26.1 (±4.3)
TR peak velocity (n = 27)2.7 (±0.4)
1.70–3.60
2.7 (±0.5)2.7 (±0.4)
n (%)n (%)n (%)
Narcotic analgesics prescribed (baseline)26 (89.7%)11 (78.6%)15 (100%)
Episodes of pain in the past 12 months
Min and max0–250–20
Median9.54
Use of hydroxyurea at baseline22 (75.9%)10 (71.4%)12 (80%)
Patient reported comorbidities
Congestive heart failure3 (9.7%)21
Chronic lung disease6 (19.4%)42
Blindness or trouble seeing4 (12.9%)40
Deafness or difficulty hearing3 (9.7%)21
Sugar diabetes, mellitus000
Asthma2 (6.5%)11
Ulcer or GI bleeding1 (3.2%)01
Arthritis or rheumatism4 (12.9%)22
Sciatic or chronic back pain6 (19.4%)33
High blood pressure (HTN)11 (35.5%)47
Angina2 (6.5%)20
Heart attack or MI3 (9.7%)30
Stroke8 (25.8%)62
Kidney disease3 (9.7%)30
Number of comorbid conditions1.8 (±1.9)2.4 (±2.2)1.3 (±1.3)
Number of medications at baseline7.4 (±4.1)8.4 (±3.9)6.5 (±4.1)

No statistically significant differences were found between groups based on the independent two-sample t-tests. Normal ranges are fetal haemoglobin = 0.0–2.0; red blood cell count = 3.93–5.22; and haematocrit = 34.1–44.9.