Threshold score for the self‐report Pediatric Distress Thermometer Rating Scale in childhood cancer patients

Patel, Sunita K.; Kim, Seong-Hyeon; Johansen, Christopher; Mullins, Wendy; Nolty, Anne; Fernandez, Nathaniel; Delgado, Nicole; Folbrecht, Jeanelle; Dekel, Noya; Meier, Adrienne M.

doi:10.1002/pon.5583

Cited by 7 publications

(4 citation statements)

References 29 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…The Pediatric Distress Thermometer is a one item screening tool that measures distress, defined as worry, anxiety, sadness, or fear, reported by the child on a visual analogue scale from 0 (no distress) to 10 (severe distress), based on the child’s experience in the previous week [ 40 ]. A recent study has identified threshold scores for children with cancer [ 42 ]. The FACES pain scale also uses a visual analogue scale to assess intensity of pain and is validated from age 4 years onwards (and caregiver proxy).…”

Section: Methods and Designmentioning

confidence: 99%

Optimising symptom management in children with cancer using a novel mobile phone application: protocol for a controlled hybrid effectiveness implementation trial (RESPONSE)

Bradford

Condon

Pitt

et al. 2021

BMC Health Serv Res

View full text Add to dashboard Cite

Background Intense and aggressive treatment regimens for most children’s cancer have achieved vast improvements in survival but are also responsible for both a high number and burden of symptoms. The use of Patient Reported Outcome Measures (PROMs) demonstrates a range of benefits for improved symptom management in adults with cancer. There are, however, multiple barriers to integrating PROMs into routine care in children and adolescents with cancer. This study aims to evaluate: (1) the effectiveness of electronic PROMs to generate stratified alerts, symptom management recommendations and graphical summaries (the RESPONSE system) to improve health outcomes and (2) the implementation of the RESPONSE system by assessing feasibility, acceptability, satisfaction, and sustainability. Methods A pragmatic hybrid II effectiveness-implementation controlled trial, using mixed methods, will be undertaken, advancing both knowledge of the effectiveness of the intervention and implementation factors. One-hundred and sixty children with cancer receiving active treatment will be recruited 1:1 to a non-randomised study involving two groups with an equal number of participants in each group. The intervention group (n = 80) will be prospectively recruited to receive the RESPONSE system intervention over eight weeks, versus the historical matched control group (n = 80) who will complete the ePROMs without access to the RESPONSE system. The primary outcome of the effectiveness trial is change between groups in total symptom burden. Secondary outcomes include child health-related quality-of-life and implementation outcomes. Trial data will be analysed using linear mixed-effects models. Formative implementation evaluation is informed by CFIR and ERIC frameworks and implementation outcomes will be mapped to the RE-AIM framework and include interviews, field notes, as well as administrative data to evaluate feasibility, acceptability, satisfaction and sustainability. Trial registration number ACTRN12621001084875. Retrospectively Registered 16 August 2021.

show abstract

Section: Methods and Designmentioning

confidence: 99%

Optimising symptom management in children with cancer using a novel mobile phone application: protocol for a controlled hybrid effectiveness implementation trial (RESPONSE)

Bradford

Condon

Pitt

et al. 2021

BMC Health Serv Res

View full text Add to dashboard Cite

show abstract

“…The United States National Comprehensive Cancer Network (NCCN) distress thermometer (DT) was developed according to these needs and it allows for a quick and easy survey of distress (Jacobsen et al 2005 ). Previous studies have shown that its use is reliable, valid and acceptable in pediatric cancer patients (Patel et al 2010 , 2011 , 2014 , 2021 ; Schulte et al 2019 ; Wiener et al 2017 ). With the help of the DT, the child can classify his or her subjectively experienced stress on a visual analog scale with the subdivisions 0 (no stress) to 10 (extreme stress).…”

Section: Introductionmentioning

confidence: 99%

Application of the National Comprehensive Cancer Network-distress thermometer in pediatric patients during autologous and allogeneic hematopoietic stem cell transplantation and relationship to blood parameters of the stress axis

Malaval,

Cabanillas Stanchi,

Werle

et al. 2023

J Cancer Res Clin Oncol

View full text Add to dashboard Cite

Purpose Hematopoietic stem cell transplantations (HSCT) are extremely stressful procedures for pediatric patients. The activation of the hypothalamic pituitary adrenocortical axis (HPA) can influence the immune system negatively and therefore the overall outcome. The distress thermometer (DT) is an easy to use tool for the self-assessment of perceived distress. Methods In this prospective study, a DT with an attached problem list was used in 40 pediatric patients undergoing HSCT and in one parent of each patient. The patients were aged 10–18 years. The patients' cortisol, thyroid stimulating hormone, free triiodothyronine and thyroxine levels were measured regularly during the in-patient stay. Results After admission to the hospital, the stress levels of the pediatric patients and their parents increased and reached their maximum on the day of HSCT. The overall stress values of the parents were higher than those of their children. There was a significant difference in the parents’ stress levels on the day of HSCT, as compared to their stress levels on other days. The mean cortisol values of the pediatric patients also increased after admission, reaching significant elevated levels above the upper normal limit 1 week after HSCT and on discharge day. Although the pediatric patients experienced mainly exhaustion, especially on the day of transplantation, their parents mainly felt worry and anxiety. Interestingly, the rate of worry among children increased in the post-transplant period and reached its maximum on the day of discharge. Conclusions In summary, a significantly increased stress level is shown for both the patients and their parents. This is reflected for the patients both in the DT scores and in the increased cortisol values. For the parents, the focus is primarily on worry and anxiety, for the patients primarily on exhaustion and worry.

show abstract

“…Outcome measures included two scales for measuring distress levels and anxiety: the Distress Thermometer [15,16] and the RCMAS-2 [17]. The Pediatric Distress Thermometer consists of a self-reported scale and has been validated as a screening tool for distress in pediatric oncology [16]. A value above 3 has been indicated as reasonable for identifying distress in children [16].…”

mentioning

confidence: 99%

“…The Pediatric Distress Thermometer consists of a self-reported scale and has been validated as a screening tool for distress in pediatric oncology [16]. A value above 3 has been indicated as reasonable for identifying distress in children [16]. The score from the RCMAS-2 scale represents the sum of the results of the whole RCMAS-2 scale and aims to detect a level of general anxiety.…”

mentioning

confidence: 99%

Feasibility of a VR Intervention to Decrease Anxiety in Children with Tumors Undergoing CVC Dressing

Russo

Tozzi

Mastronuzzi

et al. 2022

IJERPH

View full text Add to dashboard Cite

Virtual reality (VR) represents a promising digital intervention for managing distress and anxiety in children with tumors undergoing painful medical procedures. In an experimental cross-over study, we administered a VR intervention consisting of relaxing games during central venous catheter (CVC) dressing. The VR sessions were compared with no-VR during CVC medication. We used the distress thermometer and RCMAS-2 scale to assess distress and anxiety levels. We also explored the satisfaction level in patients and families. We enrolled 22 children. The distress levels after medication were lower in the VR group than in those without VR (VR: median 2; IQR 0–2; no-VR: median 4; IQR: 3–5). No variation in anxiety levels was detected by VR intervention. Satisfaction for using VR was very high in children and their families although a total of 12% of children were disappointed by the effect of VR. Most healthcare workers felt that VR would be useful in routine clinical practice. A VR intervention is highly acceptable, may be efficacious in decreasing distress in children with cancer undergoing painful procedures, but it is less likely that it has a measurable impact on anxiety. Evidence from larger studies is needed to assess VR translation into the clinical workflow.

show abstract

Threshold score for the self‐report Pediatric Distress Thermometer Rating Scale in childhood cancer patients

Cited by 7 publications

References 29 publications

Optimising symptom management in children with cancer using a novel mobile phone application: protocol for a controlled hybrid effectiveness implementation trial (RESPONSE)

Optimising symptom management in children with cancer using a novel mobile phone application: protocol for a controlled hybrid effectiveness implementation trial (RESPONSE)

Application of the National Comprehensive Cancer Network-distress thermometer in pediatric patients during autologous and allogeneic hematopoietic stem cell transplantation and relationship to blood parameters of the stress axis

Feasibility of a VR Intervention to Decrease Anxiety in Children with Tumors Undergoing CVC Dressing

Contact Info

Product

Resources

About