Dyer et al. (2013): Is reflexology as effective as aromatherapy massage for symptom relief in an adult outpatient oncology population?: Difference between revisions
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|Reference=Publication: Is reflexology as effective as aromatherapy massage for symptom relief in an adult outpatient oncology population? | |Reference=Publication: Is reflexology as effective as aromatherapy massage for symptom relief in an adult outpatient oncology population? | ||
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=Brief summary= | =Brief summary= | ||
In this comparative study, 115 patients with different types of cancer were randomly assigned to a group that received either aromatherapy massage or reflex therapy. Various quality of life parameters were recorded in both groups, including the participants' self-reporting of the negative effects of cancer on them and how these had changed as a result of treatment with aromatherapy massage/reflex therapy. It was shown that there was a significant positive development in the assessed quality of life in both arms. However, there was no difference between the groups. This study therefore shows that reflex therapy is not inferior to aromatherapy massage in terms of improving the quality of life measured here, but it is not superior either. Aromatherapy massage itself is not an established therapy that can be assumed to have an effect beyond a placebo effect. The authors also mention that there is insufficient evidence of the effectiveness of aromatherapy massage. | In this comparative study, 115 patients with different types of cancer were randomly assigned to a group that received either aromatherapy massage or reflex therapy. Various quality of life parameters were recorded in both groups, including the participants' self-reporting of the negative effects of cancer on them and how these had changed as a result of treatment with aromatherapy massage/reflex therapy. It was shown that there was a significant positive development in the assessed quality of life in both arms. However, there was no difference between the groups. This study therefore shows that reflex therapy is not inferior to aromatherapy massage in terms of improving the quality of life measured here, but it is not superior either. Aromatherapy massage itself is not an established therapy that can be assumed to have an effect beyond a placebo effect. The authors also mention that there is insufficient evidence of the effectiveness of aromatherapy massage. | ||
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|Outcome name=Well-being | |Outcome name=Well-being | ||
|Outcome specification=Qualitative responses of the patients analysed by framework analysis | |Outcome specification=Qualitative responses of the patients analysed by framework analysis | ||
|Type of measurement= | |Type of measurement=MYCaW (Measure Yourself Concerns and Wellbeing) | ||
|Results during intervention=NA | |Results during intervention=NA | ||
|Results after intervention=The most common answer to the question “What was the most important thing for you?” was “Relaxation and time for myself” in both arms | |Results after intervention=The most common answer to the question “What was the most important thing for you?” was “Relaxation and time for myself” in both arms | ||
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Latest revision as of 15:56, 30 November 2024
Reference ↗ | |
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Title | Is reflexology as effective as aromatherapy massage for symptom relief in an adult outpatient oncology population? |
Topic | Reflexology |
Author | Dyer, J, Thomas, K, Sandsund, C, Shaw, C |
Year | 2013 |
Journal | Complementary Therapies in Clinical Practice |
DOI | http://dx.doi.org/10.1016/j.ctcp.2013.03.002 |
Brief summary
In this comparative study, 115 patients with different types of cancer were randomly assigned to a group that received either aromatherapy massage or reflex therapy. Various quality of life parameters were recorded in both groups, including the participants' self-reporting of the negative effects of cancer on them and how these had changed as a result of treatment with aromatherapy massage/reflex therapy. It was shown that there was a significant positive development in the assessed quality of life in both arms. However, there was no difference between the groups. This study therefore shows that reflex therapy is not inferior to aromatherapy massage in terms of improving the quality of life measured here, but it is not superior either. Aromatherapy massage itself is not an established therapy that can be assumed to have an effect beyond a placebo effect. The authors also mention that there is insufficient evidence of the effectiveness of aromatherapy massage.
In dieser Vergleichsstudie wurden 115 Patienten verschiedener Krebserkrankungen zufällig in eine Gruppe eingeteilt, die entweder Massagen mit Aromatherpie oder Reflextherapie erhalten haben. In beiden Gruppen wurden verschiedene Parameter der Lebensqualität erhoben, darunter konnten die Teilnehmer selbst angeben, welche negativen Auswirkungen die Krebserkrankung auf sie hat und wie sich diese durch die Behandlung mit Aromatherpie-Massage/ Reflextheapie verändert haben. Dabei konnte gezeigt werden, dass es in beiden Armen eine bedeutsame positive Entwicklung der erhobenen Lebensqualität gab. Allerdings gab es keinen Unterschied zwischen den Gruppen. Diese Studie zeigt also, dass die Reflextherapie der Aromatherapie-Massage in Bezug auf die Verbesserung der hier gemessenen Lebensqualität nicht unterlegen, aber auch nicht überlegen ist. Die Aromatherapie-Massage ist selbst keine etablierte Therapie, von der man ausgehen kann, dass ihr Effekt über ein Placeboeffekt hinausgeht. Auch die Autoren erwähnen, dass es keinen ausreichenden Nachweis über die Wirksamkeit der Aromatherapie-Massage gibt.
Study Design
Prospective / Retrospective Prospective: forward-looking, examples include clinical trials, cohort studies, and long-term observational studies;</br>Retrospective: backward-looking, relying on existing data, examples include case-control studies and retrospective cohort studies | Prospective |
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Monocentric / Multicentric Monocentric: conducted in one center/ hospital; </br>Multicentric: conducted in multiple centers/ hospitals | Monocentric |
Blinding No: Open, all parties are aware of group assignments;</br>Single: one party is unaware of group assignments (generally participants);</br>Double: two parties are unaware of group assignments (generally the participants and the researchers); </br>Triple: concealing group assignment from additional parties | No |
Is randomized | Yes |
Cross-over Participants alternate between different treatment groups or conditions over a specified period, allowing each participant to serve as their own control | No |
Number of arms | 2 |
Study characteristics
Inclusion criteria | Patients over 18 years old, with a diagnosis of cancer, attending the hospital as NHS out- patients, wishing to access complementary therapy treatment and able to attend the hospital for four, one-hour sessions. |
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Exclusion criteria | Those already receiving (or who had received in the past two months or who were intending to receive during the period of the study) either aromatherapy massage or reflexology from any practitioner and those unable to receive the intervention due to contraindications or precautions for either therapy. |
N randomized | 115 |
Analysis PP: Per Protocol analysis, i.e. only participants included who adhered to the study protocol.</br>ITT: Intention-to-treat analysis, i.e. all randomized participants included regardless of any drop-outs or changes in assignment.</br>mITT: modified Intention-to-treat analysis can refer to analyses in which participants with missing outcome data are excluded or it can refer to analyses in which only participants who received at least one treatment dose are included. In this case, participants dropped out of the study prematurely for reasons unrelated to the treatment. | PP Analysis |
Specifications on analyses | One-tailed independent samples t-test |
Countries of data collection | United Kingdom - Great Britain |
LoE Level of evidence | 1b Oxford 2009 |
Outcome timeline Data collection times | T0: 1st intervention
T1: 2nd intervention T2: 3rd intervention T3: 4th intervention |
Characteristics of participants
Setting Refers to cancer therapy setting.</br>- Curative therapy: aims to completely eradicate a disease and achieve a full recovery; </br>- Neo-adjuvant therapy: form of curative therapy, given before the primary treatment for cancer (usually surgery); </br>- Adjuvant therapy: form of curative therapy, given after the primary treatment for cancer (usually surgery); </br>- Palliative therapy: focuses on providing relief from symptoms and improving the quality of life for patients, without necessarily targeting the underlying disease; </br>- Active surveillance: involves close monitoring of disease progression without any intervention (typically used for prostate cancer);</br>- No therapy setting: Patients who completed therapy/are currently not in cancer treatment, cancer survivors. | Curative |
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Types of cancer "Other Cancers" means that only a subpopulation was specified, but further unspecified cancer types were included | Breast Cancer, Gastrointestinal Cancers, Gynecologic Cancers - Ovarian Cancer, Hematologic Cancers, Head and Neck Cancers, Lung Cancer, Brain and Central Nervous System (CNS) Cancers, Skin Cancer, Other Cancers, Unspecified Sarcoma, Genitourinary Cancers |
Cancer stages Early Stage: generally refers to cancer that is localized to the area where it started, mostly stages I and II;</br>Advanced Stage: cancer that has spread beyond its original site, mostly stages III and IV, with stage IV indicating distant metastasis | NI |
Specifications on cancer stages | NI |
Comorbidities | NI |
Current cancer therapies | NI |
Specifications on cancer therapies | NI |
Previous cancer therapies | NI |
Gender | Mixed |
Gender specifications | 93 % female |
Age groups | Adults (18+) |
Age groups specification | Mean (SD): Arm A: 53.76 (11.36); Arm B: 54.72 (11.12) |
Arms
Arm type Active control: group receives active treatment; </br>Passive control: for example treatment as usual, waiting control, no treatment | Placebo |
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Number of participants (arm) N randomized | 58 |
Drop-out Number of participants who left the study for any reason or did not provide information on every data collection date | N=4 |
Drop-out reasons | No subdivision between arms:
2nd intervention: Caring for family member (n=1); too difficult to attend appointments (n=2); caring for a friend (n=1) 3rd intervention: Withdrew: for further medical treatment (n=1); RIP (n=1) 4th intervention: Withdrew: unable to attend (n=1); Did not attend (n=1); admitted as inpatient (n=1); caring for a friend (n=1); felt too unwell to continue (n=1 |
Intervention | Aromatherapy massage |
Dosage and regime | 4 sessions for 1 h each, spread over an average of 10 weeks |
One-time application | No |
Duration in days For long-term interventions, the number of days is an estimation.</br>A value of -999 indicates that the exact duration cannot be extracted from the study due to ambiguous or incomplete information. See Outcome timeline or Dosage and regime for further information. | 70 |
Side effects / Interactions | NI |
Arm type Active control: group receives active treatment; </br>Passive control: for example treatment as usual, waiting control, no treatment | Intervention |
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Number of participants (arm) N randomized | 57 |
Drop-out Number of participants who left the study for any reason or did not provide information on every data collection date | N=7 |
Drop-out reasons | No subdivision between arms:
2nd intervention: Caring for family member (n=1); too difficult to attend appointments (n=2); caring for a friend (n=1) 3rd intervention: Withdrew: for further medical treatment (n=1); RIP (n=1) 4th intervention: Withdrew: unable to attend (n=1); Did not attend (n=1); admitted as inpatient (n=1); caring for a friend (n=1); felt too unwell to continue (n=1 |
Intervention | Reflex therapy |
Dosage and regime | 4 sessions, no information regarding duration of therapy |
One-time application | No |
Duration in days For long-term interventions, the number of days is an estimation.</br>A value of -999 indicates that the exact duration cannot be extracted from the study due to ambiguous or incomplete information. See Outcome timeline or Dosage and regime for further information. | 70 |
Side effects / Interactions | NI |
Outcomes
Well-being
Outcome type As specificed by the authors | Primary |
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Outcome specification | Overall well-being scores and levels of relaxation.
Before the first and after the last session: main complaints according to own statement |
Type of measurement | MYCaW (Measure Yourself Concerns and Wellbeing) |
Results during intervention - Results during intervention means that the time of data collection is during or shortly after the period of the intervention (e.g. on the last day or a few days after). The results therefore still relate to the direct effects of the intervention.</br>- Results after intervention means there is a longer break between the time of data collection and the end of the intervention, e.g. more than a week. The results relate more to long-term effects.</br>- If a categorization in Results during vs. after intervention is not possible (e.g. survival data), the results are summarized under Results after intervention under the headline "Overall". | NA |
Results after intervention - Results during intervention means that the time of data collection is during or shortly after the period of the intervention (e.g. on the last day or a few days after). The results therefore still relate to the direct effects of the intervention.</br>- Results after intervention means there is a longer break between the time of data collection and the end of the intervention, e.g. more than a week. The results relate more to long-term effects.</br>- If a categorization in Results during vs. after intervention is not possible (e.g. survival data), the results are summarized under Results after intervention under the headline "Overall". | Mean difference 0.453 (SE = 0.323) in favor of aromatherapy, but this is significantly less than one point on the scale (p=0.046). |
Risk of Bias Assessment: Cochrane RoB tool 2.0 | |
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Bias arising from the randomization process | ? |
Bias due to deviation from intended intervention (assignment to intervention) | ? |
Bias due to deviation from intended intervention (adhering to intervention) | NA |
Bias due to missing outcome data | ? |
Bias in measurement of the outcome | ? |
Bias in selection of the reported result | ? |
Other sources of bias | ? |
Overall RoB judgment | ? |
Well-being
Outcome type As specificed by the authors | Secondary |
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Outcome specification | Secondary complaints according to self-report |
Type of measurement | MYCaW (Measure Yourself Concerns and Wellbeing) |
Results during intervention - Results during intervention means that the time of data collection is during or shortly after the period of the intervention (e.g. on the last day or a few days after). The results therefore still relate to the direct effects of the intervention.</br>- Results after intervention means there is a longer break between the time of data collection and the end of the intervention, e.g. more than a week. The results relate more to long-term effects.</br>- If a categorization in Results during vs. after intervention is not possible (e.g. survival data), the results are summarized under Results after intervention under the headline "Overall". | NA |
Results after intervention - Results during intervention means that the time of data collection is during or shortly after the period of the intervention (e.g. on the last day or a few days after). The results therefore still relate to the direct effects of the intervention.</br>- Results after intervention means there is a longer break between the time of data collection and the end of the intervention, e.g. more than a week. The results relate more to long-term effects.</br>- If a categorization in Results during vs. after intervention is not possible (e.g. survival data), the results are summarized under Results after intervention under the headline "Overall". | Significant and clinically relevant improvement in both arms (reflex therapy: M= -1.44 [95%CI: -1.90, -0.97]; p= NI; aroma massage: M= -1.98 [95%CI: -2.49,-1.47]; p= NI), but no significant arm differences (M= 0.54 ([95%CI: -0.14, 1.22]; p= NI) |
Risk of Bias Assessment: Cochrane RoB tool 2.0 | |
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Bias arising from the randomization process | ? |
Bias due to deviation from intended intervention (assignment to intervention) | ? |
Bias due to deviation from intended intervention (adhering to intervention) | NA |
Bias due to missing outcome data | ? |
Bias in measurement of the outcome | ? |
Bias in selection of the reported result | ? |
Other sources of bias | ? |
Overall RoB judgment | ? |
Well-being
Outcome type As specificed by the authors | Secondary |
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Outcome specification | Fundamental well-being |
Type of measurement | MYCaW (Measure Yourself Concerns and Wellbeing) |
Results during intervention - Results during intervention means that the time of data collection is during or shortly after the period of the intervention (e.g. on the last day or a few days after). The results therefore still relate to the direct effects of the intervention.</br>- Results after intervention means there is a longer break between the time of data collection and the end of the intervention, e.g. more than a week. The results relate more to long-term effects.</br>- If a categorization in Results during vs. after intervention is not possible (e.g. survival data), the results are summarized under Results after intervention under the headline "Overall". | NA |
Results after intervention - Results during intervention means that the time of data collection is during or shortly after the period of the intervention (e.g. on the last day or a few days after). The results therefore still relate to the direct effects of the intervention.</br>- Results after intervention means there is a longer break between the time of data collection and the end of the intervention, e.g. more than a week. The results relate more to long-term effects.</br>- If a categorization in Results during vs. after intervention is not possible (e.g. survival data), the results are summarized under Results after intervention under the headline "Overall". | Significant and clinically relevant improvement over time in both arms (reflexology: M= -0.70 [95% CI: -1.16, -0.24]; aromatherapy massage: M= -1.16 [95% CI: -1.15, -0.80]), but no sig. arm differences (M= 0.45 [95% CI: -0.12, 1.03]; p=NI). |
Risk of Bias Assessment: Cochrane RoB tool 2.0 | |
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Bias arising from the randomization process | ? |
Bias due to deviation from intended intervention (assignment to intervention) | ? |
Bias due to deviation from intended intervention (adhering to intervention) | NA |
Bias due to missing outcome data | ? |
Bias in measurement of the outcome | ? |
Bias in selection of the reported result | ? |
Other sources of bias | ? |
Overall RoB judgment | ? |
Relaxation
Outcome type As specificed by the authors | Secondary |
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Outcome specification | Before and after the 4 sessions: Change in values before and after treatment at the respective 4 points in time |
Type of measurement | VAS (Visual Analogue Scale) |
Results during intervention - Results during intervention means that the time of data collection is during or shortly after the period of the intervention (e.g. on the last day or a few days after). The results therefore still relate to the direct effects of the intervention.</br>- Results after intervention means there is a longer break between the time of data collection and the end of the intervention, e.g. more than a week. The results relate more to long-term effects.</br>- If a categorization in Results during vs. after intervention is not possible (e.g. survival data), the results are summarized under Results after intervention under the headline "Overall". | NA |
Results after intervention - Results during intervention means that the time of data collection is during or shortly after the period of the intervention (e.g. on the last day or a few days after). The results therefore still relate to the direct effects of the intervention.</br>- Results after intervention means there is a longer break between the time of data collection and the end of the intervention, e.g. more than a week. The results relate more to long-term effects.</br>- If a categorization in Results during vs. after intervention is not possible (e.g. survival data), the results are summarized under Results after intervention under the headline "Overall". | No significant difference between the arms (p= 0.489) |
Risk of Bias Assessment: Cochrane RoB tool 2.0 | |
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Bias arising from the randomization process | ? |
Bias due to deviation from intended intervention (assignment to intervention) | ? |
Bias due to deviation from intended intervention (adhering to intervention) | NA |
Bias due to missing outcome data | ? |
Bias in measurement of the outcome | ? |
Bias in selection of the reported result | ? |
Other sources of bias | ? |
Overall RoB judgment | ? |
Relaxation
Outcome type As specificed by the authors | Secondary |
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Outcome specification | Change in values across all 4 time points, arm comparison |
Type of measurement | VAS (Visual Analogue Scale) |
Results during intervention - Results during intervention means that the time of data collection is during or shortly after the period of the intervention (e.g. on the last day or a few days after). The results therefore still relate to the direct effects of the intervention.</br>- Results after intervention means there is a longer break between the time of data collection and the end of the intervention, e.g. more than a week. The results relate more to long-term effects.</br>- If a categorization in Results during vs. after intervention is not possible (e.g. survival data), the results are summarized under Results after intervention under the headline "Overall". | NA |
Results after intervention - Results during intervention means that the time of data collection is during or shortly after the period of the intervention (e.g. on the last day or a few days after). The results therefore still relate to the direct effects of the intervention.</br>- Results after intervention means there is a longer break between the time of data collection and the end of the intervention, e.g. more than a week. The results relate more to long-term effects.</br>- If a categorization in Results during vs. after intervention is not possible (e.g. survival data), the results are summarized under Results after intervention under the headline "Overall". | No significant difference between the arms (p= 0.408) |
Risk of Bias Assessment: Cochrane RoB tool 2.0 | |
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Bias arising from the randomization process | ? |
Bias due to deviation from intended intervention (assignment to intervention) | ? |
Bias due to deviation from intended intervention (adhering to intervention) | NA |
Bias due to missing outcome data | ? |
Bias in measurement of the outcome | ? |
Bias in selection of the reported result | ? |
Other sources of bias | ? |
Overall RoB judgment | ? |
Well-being
Outcome type As specificed by the authors | Secondary |
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Outcome specification | Percentage of patients who have an improvement on at least one scale of the MYCaW, arm comparison |
Type of measurement | MYCaW (Measure Yourself Concerns and Wellbeing) |
Results during intervention - Results during intervention means that the time of data collection is during or shortly after the period of the intervention (e.g. on the last day or a few days after). The results therefore still relate to the direct effects of the intervention.</br>- Results after intervention means there is a longer break between the time of data collection and the end of the intervention, e.g. more than a week. The results relate more to long-term effects.</br>- If a categorization in Results during vs. after intervention is not possible (e.g. survival data), the results are summarized under Results after intervention under the headline "Overall". | NA |
Results after intervention - Results during intervention means that the time of data collection is during or shortly after the period of the intervention (e.g. on the last day or a few days after). The results therefore still relate to the direct effects of the intervention.</br>- Results after intervention means there is a longer break between the time of data collection and the end of the intervention, e.g. more than a week. The results relate more to long-term effects.</br>- If a categorization in Results during vs. after intervention is not possible (e.g. survival data), the results are summarized under Results after intervention under the headline "Overall". | Arm A: 82% to 91% on the various scales, Arm B = 68% to 86% on the various scales. No significant arm differences |
Risk of Bias Assessment: Cochrane RoB tool 2.0 | |
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Bias arising from the randomization process | ? |
Bias due to deviation from intended intervention (assignment to intervention) | ? |
Bias due to deviation from intended intervention (adhering to intervention) | NA |
Bias due to missing outcome data | ? |
Bias in measurement of the outcome | ? |
Bias in selection of the reported result | ? |
Other sources of bias | ? |
Overall RoB judgment | ? |
Well-being
Outcome type As specificed by the authors | Secondary |
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Outcome specification | Qualitative responses of the patients analysed by framework analysis |
Type of measurement | MYCaW (Measure Yourself Concerns and Wellbeing) |
Results during intervention - Results during intervention means that the time of data collection is during or shortly after the period of the intervention (e.g. on the last day or a few days after). The results therefore still relate to the direct effects of the intervention.</br>- Results after intervention means there is a longer break between the time of data collection and the end of the intervention, e.g. more than a week. The results relate more to long-term effects.</br>- If a categorization in Results during vs. after intervention is not possible (e.g. survival data), the results are summarized under Results after intervention under the headline "Overall". | NA |
Results after intervention - Results during intervention means that the time of data collection is during or shortly after the period of the intervention (e.g. on the last day or a few days after). The results therefore still relate to the direct effects of the intervention.</br>- Results after intervention means there is a longer break between the time of data collection and the end of the intervention, e.g. more than a week. The results relate more to long-term effects.</br>- If a categorization in Results during vs. after intervention is not possible (e.g. survival data), the results are summarized under Results after intervention under the headline "Overall". | The most common answer to the question “What was the most important thing for you?” was “Relaxation and time for myself” in both arms |
Risk of Bias Assessment: Cochrane RoB tool 2.0 | |
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Bias arising from the randomization process | ? |
Bias due to deviation from intended intervention (assignment to intervention) | ? |
Bias due to deviation from intended intervention (adhering to intervention) | NA |
Bias due to missing outcome data | ? |
Bias in measurement of the outcome | ? |
Bias in selection of the reported result | ? |
Other sources of bias | ? |
Overall RoB judgment | ? |
Funding and Conflicts of Interest
Funding | A grant from the Royal Marsden Hospital Charity Panel pro- vided the funding for the Data Manager who manages data for studies conducted by the Therapies Department (CP08201). There was no other funding for this study. |
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Conflicts of Interest | The authors have no conflicts of interest related to this work. |
Further points for assessing the study
Sample
Power analysis performed | ? |
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- Sample size corresponds to power analysis | ? |
- Reasons for insufficient sample size based on power analysis | ? |
If no power analysis performed: at least moderate sample size (n >= 30 per arm) | ? |
Ethnicity mentioned | ? |
Alternative Explanation
Other explanations for an effect besides the investigated intervention | ? |
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- Possibility of attention effects | ? |
- Possibility of placebo effects | ? |
- Other reasons | ? |
Statistics
Correct use of parametric and non-parametric tests Testing for normal distribution only necessary if parametric tests are used, NI: use of parametric tests without report of normal distribution testing | ? |
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Correction for multiple testing | ? |
Measurement of compliance | ? |
Consistent reporting in numbers (figures, flowchart, abstract, results) | ? |
Comprehensive and coherent reporting | ? |
Cross-over | ? |
- Sufficient washout period | ? |
- Tested for carry-over effects | ? |
- Tested for sequence effects | ? |
Interpretation of results
Effect sizes reported (clinical vs. statistical significance) | ? |
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Side effects systematically recorded | ? |
Side effects considered in result interpretation | ? |
Ethics votum | ? |