Nurse-led telehealth interventions for symptom management in patients with cancer receiving systemic or radiation therapy: a systematic review and meta-analysis

Abstract

Purpose

Patients receiving cancer treatments experience many treatment-related symptoms. Telehealth is increasingly being used to support symptom management. The overall aim was to determine the effectiveness of nurse-led telehealth symptom management interventions for patients with cancer receiving systemic or radiation therapy compared to usual care on health service use, quality of life, and symptom severity.

Methods

A systematic review was conducted following the Cochrane Handbook and PRISMA reporting guidelines. Five electronic databases were searched. Two independent reviewers screened articles and extracted data. Meta-analysis was performed if data were clinically and methodologically homogeneous. Subanalysis was conducted on reactive and scheduled telehealth interventions.

Results

Of 7749 citations screened, 10 studies were included (8 randomized control trials, 2 quasi-experimental). Five were reactive telehealth interventions with patient-initiated contact and five evaluated scheduled telehealth interventions initiated by nurses. Compared to usual care (typically patient-initiated calls), nurse-led telehealth interventions for symptom management showed no statistically significant difference in hospitalizations, emergency department visits, or unscheduled clinic visits. Two of three studies of reactive telehealth interventions showed improved quality of life. All telehealth interventions showed reduction in the severity of most symptoms. Pain severity was significantly reduced (standard mean difference − 0.54; 95% CI − 0.88, − 0.19). Significant heterogeneity prevented meta-analysis for most outcomes.

Conclusion

Few studies evaluated nurse-led telehealth interventions for cancer symptom management. Compared to usual care, patients exposed to telehealth interventions had reduced symptom severity and no difference in health services use. Future research should focus on better reporting intervention characteristics and consistently measuring outcomes.

Supplementary Information

The online version contains supplementary material available at 10.1007/s00520-022-07052-z.

Introduction

While undergoing cancer treatment, patients often experience treatment-related symptoms such as fatigue, pain, nausea, constipation, or anxiety [1, 2]. Symptoms are typically monitored during regularly scheduled clinic visits or patients reach out to their clinical team if they have concerns between visits. Given symptoms can affect patients’ daily function and can escalate quickly to be life-threatening, patients often have unscheduled clinic visits, emergency department (ED) visits, hospitalizations, and reduced quality of life (QOL) [3–7]. Hence, symptom management is an essential part of patients’ care throughout treatment and requires collaboration between healthcare professionals and patients [8].

Remote symptom management is provided through telehealth services, where patients can connect at a distance with their healthcare providers between clinic visits. Although telehealth has been used for years, the demand has grown exponentially in the wake of the worldwide COVID-19 pandemic with the need to limit potential exposure, especially for those with high-risk conditions such as cancer [9]. It is therefore important to determine if telehealth is an effective approach for care in the cancer population.

Telehealth uses forms of communication or information technologies to provide remote healthcare to patients [10]. A range of technologies such as telephones, mobile phones, internet-based and smartphone applications have been used for patients with cancer [11–17]. Telehealth interventions can come in two forms, (1) pre-scheduled communications based on the timing of treatments, typically initiated by the healthcare provider (scheduled interventions), or (2) symptom response communications by the healthcare providers in response to a patient-initiated phone call or an automated alert, triggered by a patient’s self-assessment exceeding a pre-defined threshold (reactive interventions). Patient self-reported outcome (PRO) measures which generate the automated alerts have been shown to improve patient-provider communication and patient satisfaction [18–20].

Nurses typically provide telehealth services, including responding to automated alerts, assessing symptom severity, guiding patients in self-care, and triaging those with severe symptoms [21]. Nurse-led telehealth interventions for patients with cancer have been reported to improve patient’s self-care, provide more timely access to resources for symptom management and healthcare professionals, and increase convenience and flexibility [22–24]. Despite this, little is known about the effect of telehealth interventions on health service utilization (HSU) and QOL [19, 25–27]. Furthermore, previous systematic reviews have focused on specific types of telehealth interventions (telephone or internet-based), have been limited by cancer type, or only included participants being monitored for recurrence once treatment was completed [19, 27–30].

The overall aim was to determine the effectiveness of nurse-led telehealth symptom management interventions (I) for patients with cancer receiving systemic or radiation therapy (P) compared to usual care (C) on HSU, QOL, and symptom severity (O).

Methods

A systematic review was conducted using the Cochrane Handbook for Systematic Reviews and Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) following an a priori protocol [31, 32].

Eligibility criteria

Based on the PICOS framework, the population of interest (P) was patients with cancer, including all tumor types and stages of disease, receiving systemic (chemotherapy, targeted therapy, immunotherapy, hormonal therapy) or radiation therapy within 4 weeks of study enrollment. There were no participant age restrictions. Interventions (I) included nurse-led telehealth interventions (telephone calls, video technology, emails, web-based systems, text messaging, mobile applications) for cancer symptom monitoring and management [10]. Studies that delivered the intervention by healthcare professionals other than nurses or nurse practitioners (NPs) or included a non-outpatient intervention were excluded. The comparator (C) was usual care. If the control group included another form of telehealth intervention, the study was excluded. The primary outcome (O) was HSU (ED visits, unscheduled hospitalization, unplanned clinic visits). Secondary outcomes included QOL and symptom severity. Included study designs (S) were experimental (quantitative randomized control trials (RCTs), quasi-randomized control trials, non-randomized control trials, and quasi-experimental (controlled before-after (CBA)) and controlled interrupted time series with no date limits. These designs allow for direct comparison of treatment to standard of care while minimizing bias. The study duration was restricted to studies that were at least 4 weeks. Conference abstracts, theses, and dissertations were excluded. Only studies in English were included.

Search strategy and study selection

We searched MEDLINE via OVID, Embase via OVID, Cochrane Central Register of Controlled Trials (CENTRAL); CINAH; PsycINFO; and clinicalTrials.gov (Online Resource 1) as of March 10, 2021, for relevant citations using individualized search strategies for each database. Citations from each database search were exported to Covidence for removing duplicates and screening [33]. Two reviewers (CK, CD, NM) independently screened titles and abstracts for eligibility, and then full-text articles identified for inclusion. At each step, consensus was reached by group discussion to resolve disagreements.

Data extraction

Two reviewers individually extracted data from all included studies, using a standardized data extraction template adapted from the Cochrane handbook [31]. This included study characteristics (study design, aim), participant characteristics (age, gender, cancer type, cancer treatment, inclusion and exclusion criteria), study eligibility, details of telehealth intervention (mode of delivery—telephone, text, web-based application, etc.; healthcare provider respondent—nurse or NP), outcomes measured (HSU, QOL, symptoms), instruments used, results of outcomes including timing of measurement, conflicts of interest, and funding sources. The intervention characteristics were synthesized into a TIDieR table including intervention of interest; intervention (materials and procedures); comparator; provider of intervention; mode of delivery; when and how much; and tailoring [34].

Risk of bias in individual studies

To assess for risk of bias, two reviewers independently appraised the included studies. The Cochrane Collaboration 7-item tool was used to evaluate RCTs (Figs. 1 and 2) [35]. The ROBINS-I tool was used to evaluate non-randomized studies in 7 domains and to assess bias overall [36].

Fig. 1.

Risk of bias graph: review authors’ judgements about each risk of bias item presented as percentages across all included randomized controlled trials

Fig. 2.

Risk of bias summary: review authors’ judgements about each risk of bias item for each included randomized control trial

Data analysis

Data was analyzed in accordance with the Cochrane Handbook for Systematic Reviews of Interventions using Review Manager software (RevMan, version 5.4) [31]. HSU was assessed as total number of visits, while post-intervention QOL and symptom scores were extracted as means and standard deviations. The number of patients who provided data for each assessment was extracted, and when ranges were provided, the upper limit was taken to give the most conservative denominator.

Meta-analysis was performed if data was clinically and methodologically homogeneous. Due to different scales used for outcome measures, random-effects models with inverse variance weighting were used to calculate standard mean differences (SMD), with 95% confidence intervals (CIs) in outcomes between intervention and control groups. RCTs and quasi-randomized studies were analyzed separately. Where outcomes were assessed at multiple time points, values from similar post-intervention time points were chosen for analysis. Significant statistical heterogeneity was considered if I² was greater than 50%, and in such cases, subgroup analyses were performed to assess for possible causes and effects of heterogeneity [31]. Subgroup analysis was performed if data was available, based on the type of telehealth intervention (scheduled vs reactive intervention). Sensitivity analysis was performed to determine the effect of excluding studies with high risk of bias.

When there was insufficient reporting of an outcome or differences in outcome measures (e.g., total days of symptoms rather than symptom scores), such that data could not be combined for meta-analysis, a descriptive synthesis of the outcome was reported. Certainty of findings was evaluated using the GRADE Working Group grades of evidence [37].

Deviations from protocol

There were two deviations from the protocol. Conference abstracts were excluded due to absence of peer review. As a result of limited study numbers, all instruments to measure outcomes were included in this review and none was excluded based on having limited psychometric properties.

Results

In the search completed on March 21, 2021, there were 7749 citations after duplicates were removed, 178 full-text studies were assessed, and 10 were included (Fig. 3) [11, 14, 17, 23, 38–43]. The most common reasons for exclusion during full-text review were trial protocols or ineligible interventions (Online Resource 1). Reviewing the references of the included studies and relevant systematic reviews did not reveal any additional studies.

Fig. 3.

Study flow diagram

Study characteristics

Eight RCTs and 2 quasi-experimental studies (CBA design) were included, which evaluated 2315 participants (Table 1). Five studies were conducted in the USA [11, 17, 41–43] and one each in Canada [14], France [38], Italy [39], Hong Kong [23], and Turkey [40]. Seven studies evaluated heterogeneous samples of patients with cancer, two studies included patients with lung cancer [40, 43], and one study included women with breast cancer [23]. Nine studies evaluated adults (18 years or older) [11, 17, 23, 38–43] and one study evaluated adolescents (12–18 years) [14].

Table 1.

Characteristics of included studies

Study	Participants	Intervention	Outcomes of interest
Scheduled interventions
Bouleftour 2021 [38] RCT, France	184 adults with solid or hematologic malignancy initiating oral chemotherapy • Intervention: n = 92, median (IQR) age 68 (60–78) years, female 43 (46.7%) • Control: n = 91, median (IQR) age 73 (65–78) years, female 40 (44%)	Pre-scheduled nurse-led telephone calls	Hospitalizations, QOL, symptom severity
Cirillo 2020 [39] RCT, Italy	432 adults with any cancer initiating oral chemotherapy • Intervention: n = 212, mean (SD) age 68.9 (10.9) years, female 92 (50%) • Control: n = 220, mean (SD) age 69.9 (10.1) years, female 95 (49%)	Pre-scheduled nurse-led telephone calls	(Unscheduled and avoidable) clinic visits and ED visits*, symptom severity
Lai 2019 [23] RCT, Hong Kong	120 females with stage I to III breast cancer starting chemotherapy • Intervention: n = 58, mean (SD) age 51.55 (8.82) years • Control: n = 62, mean (SD) age 50.58 (9.25) years	Pre-scheduled nurse-led telephone calls	QOL*, symptom severity
Traeger 2015 [42] RCT, USA	120 adults with non-metastatic breast, colorectal, or lung cancer starting chemotherapy • Intervention: n = 60, 44 (73.3%) < 65 years old, female 44 (73.3%) • Control: n = 60, 41 (68.3%) < 65 years old, female 44 (73.3%)	Pre-scheduled NP-led telephone calls	Symptom severity*
Hintistan 2017 [40] Before-after study, Turkey	80 adults with stage I to III lung cancer on chemotherapy • Intervention: n = 30, ≤ 49 years 8 (26.7%), 50–59 years 15 (50%), ≥ 60 years 7 (23.3%), female 6 (20%) • Control: n = 30, ≤ 49 years: 7 (23.3%), 50–59 years: 8 (26.7%), ≥ 60 years: 15 (50%), female 4 (13.3%)	Pre-scheduled nurse-led telephone calls	QOL, symptom severity*
Reactive interventions
Basch 2016 [17] RCT, USA	539 adults with metastatic breast, genitourinary, gynecologic, or lung cancer on chemotherapy • Intervention: n = 286, median (IQR) age 59 (30–85) years, female 184 (64%) • Control: n = 253, median (IQR) age 60 (26–88) years, female 152 (60%)	Symptom reporting via web-based interface	ED visits, hospitalizations, QOL*
Kornblith 2006 [41] RCT, USA	189 adults with advanced stage breast, colon, or prostate cancer on treatment • Intervention: n = 69, mean (SD) age 73 (5.7) years, female 48 (33%) • Control: n = 62, mean (SD) age 74 (6.8) years, female 47 (29%)	Pre-scheduled telephone calls with non-nurse trained monitors	QOL, symptom severity*
Mooney 2017 [11] RCT, USA	358 adults with any cancer starting chemotherapy • Intervention: n = 180, mean (SD) age 54.77 (12.17) years, female 135 (75%) • Control: n = 178, mean (SD) age 56.79 (10.54) years, female 135 (76%)	Symptom reporting via telephone voice reporting system	Symptom severity*
Yount 2014 [43] RCT, USA	253 adults with stage III or IV lung cancer on chemotherapy • Intervention: n = 123, mean (SD) age 61 (10.3) years, male 57 (46.3%) • Control: n = 130, mean (SD) age 60.2 (10.1) years, male 68 (52.3%)	Symptom reporting via telephone keypad system	Unscheduled clinic visits, ED visits, hospitalizations, QOL, symptom severity
Jibb 2017 [14] Before-after study, Canada	40 adolescents diagnosed with cancer having pain • Mean (SD) age 14.2 (1.7) years, female 17 (43%)	Symptom reporting via web-based smartphone application	QOL, symptom severity

RCT randomized control trial, IQR interquartile range, QOL quality of life, ED emergency department

^*Primary outcome

In five studies, nurses or NPs were alerted if self-reported symptoms increased rapidly or were above a pre-defined threshold (reactive intervention) [11, 14, 17, 41, 43]. In the other five studies, nurses or NPs contacted patients at pre-defined times (scheduled interventions) [23, 38–40, 42]. Scheduled interventions only used the telephone as a mode of delivery, whereas reactive interventions used telephone-, web-, or smartphone-based systems. Two studies included symptom monitoring in the control arms but the self-reported symptom levels were not provided to the participant’s care team and did not trigger any response, thereby meeting the inclusion criteria [11, 43]. The other control arms addressed symptoms at scheduled clinic visits or by patient-initiated telephone calls. The timing of symptom monitoring and management was highly variable, ranging in frequency from twice daily to monthly (Table 2). Studies also varied in duration from 28 days to 6 months.

Table 2.

Characteristics of telehealth interventions

Scheduled nurse-initiated telehealth interventions
	Bouleftour 2021[38] RCT, France	Cirillo 2020[39] RCT, Italy	Lai 2019[23] RCT, Hong Kong	Traeger 2015[42] RCT, USA	Hintistan 2017[40] CBA, Turkey
Intervention of interest	Pre-scheduled nurse telephone calls	Pre-scheduled nurse telephone calls	Pre-scheduled nurse telephone calls	Pre-scheduled NP telephone calls	Pre-scheduled nurse researcher telephone calls
Intervention description	Aim was to give management strategies and support patients to better manage potential toxicities	Aim was to increase patients’ awareness about oral drug intake, cycle duration, toxicity, management of side effects Daily diary: calendar to check daily pill consumption and self-report specific toxicity	Pre-chemotherapy nurse consultation and telephone follow-ups during chemotherapy	Proactive calls for guidance and support during the first 2 chemotherapy cycles	Calls guided by the Nurse Care Guide that included suggestions for relief of common symptoms of lung cancer due to chemotherapy
Who provided the intervention	4 trained nurses, following a standard operating procedure	Trained nurse staff. Reference physician was always available if needed	3 experienced nurses (worked in oncology for 10 to 17 years)	The participant’s NP	4 nurse researchers with lung cancer-specific training
Telehealth intervention: when and how much	Call weeks: 1, 2, 3, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24	Calls planned on day 7 and day 14 of the 1st cycle and day 14 of 2nd cycle. If treatment discontinued and side effect ≥ grade 2, a referent physician was informed	3 calls consisting of assessment, triage, care delivery, and evaluation	Calls 1 to 3 days and 4 to 6 days post 1st and 2nd cycle. After each call, the NP documented assessment and plan of care	Calls within a week after each chemotherapy session to assess and advise participant symptoms. If symptoms not improved or new concerns, these would be reviewed at later follow-up
Usual care comparator	5 in-person medical consultations	At medical visit, physicians gave patients information and written material about drugs and the treatment plan	Brief education session before chemotherapy, care on the days of drug administration, and access to a patient-initiated hotline service during chemotherapy	Medical visit on the first day of each chemotherapy cycle and then call the clinic as needed with symptom management questions	Nurses Care Guide
Tailoring	Not reported	Patients monitored for the first two cycles regardless of the treatment schedule	Tailored to 4-cycle chemotherapy or 6-cycle chemotherapy	Not reported	Participants were encouraged to call nurse researchers as needed
Reactive patient-initiated telehealth interventions
	Basch 2016[17] RCT, USA	Kornblith 2006[41] RCT, USA	Mooney 2017[11] RCT, USA	Yount 2014[43] RCT, USA	Jibb 2017[14] CBA, Canada
Intervention of interest	Symptom reporting via web-based interface	Pre-scheduled telephone calls with trained monitors	Symptom reporting via telephone voice reporting system	Symptom reporting via telephone keypad system	Symptom reporting via web-based smartphone application
Intervention description	Self-reporting conducted via STAR (Symptom Tracking and Reporting) web-based interface of 12 symptoms (0–4 scale). Completed reports remotely and at medical oncology/infusion sites via either wireless touchscreen tablet computers or freestanding computer kiosks. Triggered e-mail alerts for nurse to contact patient if symptoms worsened by ≥ 2 points or were ≥ grade 3	Telephone calls from centralized, trained monitors. If patients scored above cutoff levels, monitor informed oncology nurse at treating institution within 24 h, who then contacted patient and made treatment recommendations Education materials: Support for People with Cancer and the People who Care about Them, Eating Hints for Cancer Patients, and Helping Hand and disease-specific information	Patients reported severity of 11 symptoms using an automated monitoring Symptom Care at Home (SCH) system. Received automated self-management coaching tailored to reported symptom prevalence and severity and NP telephone follow-up for poorly controlled symptoms	Telephone-based interactive voice response technology symptom monitoring system including 13-item symptom survey (FACT Lung Symptom Index). Any responses meeting a pre-defined threshold for a symptom generated an e-mail “alert” to the site nurse who contacted participants within one business day to assess the symptom and provide clinical care	Pain Squad+ a web-based smartphone application using a 22-item survey to assess adolescent cancer pain. If pain reported, real-time self-management recommendations provided and advised to reassess pain in 1 h. If pain score more than 3/10 on three consecutive occasions, an email alert was sent to trained nurses who contacted the adolescent and initiated provider-driven intervention such as medications changes
Who provided the intervention	Nurse was alerted to provide care when symptoms worsened	Trained telephone monitors who would refer to oncology nurses	Automated phone calls with study-based NP	Site nurses provided telephone-based follow-up	Nurse contacted the patient when significant pain was detected
Telehealth intervention when and how much	Patients received weekly e-mail reminders for between-visit reporting; nurse called participants if alerted to severe symptoms	1 telephone call each month for 6 months by monitor; nurse called participants if alerted to severe symptoms	Patients called SCH daily; NPs called participants if alerted to severe symptoms	Patients monitored and reported symptoms weekly; nurse called participants if alerted to severe symptoms	Patients completed pain assessments twice daily for 28 days
Usual care comparator	Symptoms discussed during medical visit. Patients encouraged to initiate telephone contact between visits for concerning symptoms	Education materials and nurse evaluations at study entry, 6 months, and 9 months	Called the automated symptom reporting system daily and reported presence and severity of the 11 symptoms. Were reminded to call their provider for concerns	Telephone based symptom monitoring without automated reports and paper copies	One-group baseline versus post-study design
Tailoring	Intervention continued until treatment completed	Not reported	Not reported	Not reported	May also complete ad hoc pain assessment using a truncated 8-item survey anytime between the morning and evening assessments

RCT randomized control trial, NP nurse practitioner

Most studies received funding from hospitals, universities, or national-level granting agencies [11, 14, 17, 23, 38, 40–43]. One study reported industry funding [38], and another did not report funding [39].

Quality of the evidence

Risk of bias assessments of RCTs can be found in Figs. 1 and 2. Due to the nature of the telehealth intervention, nearly all studies were high risk due to limitations in blinding participants. Many studies did not clearly state if HSU information was collected from administrative databases or provided by participants [38, 39, 43]. Basch et al. collected admissions data through medical records, but did not provide clear results on this outcome [17]. Kornblith et al. had a high number of participant dropouts prior to baseline assessment and throughout the study leading to high risk of bias for outcome reporting [41].

Both CBA studies were rated as critical risk of bias as neither commented on attempt to control for possible confounders [14, 40] (Table 3). Outcome measurements were judged to be at serious risk of bias as patients and assessors likely knew if they were in the before or after portion of the study.

Table 3.

ROBINS-I (risk of bias judgements in non-randomized studies of interventions)

	Confounding	Selection of participants	Classification of interventions	Deviations from intended interventions	Missing data	Measurement of outcomes	Selection of reported results	Overall
Hintistan 2017 [40]	Critical	Serious	Low	Low	Moderate	Serious	Low	Critical
Jibb 2017 [14]	Critical	Low	Low	Low	Moderate	Serious	Low	Critical

Four levels for risk of bias: low, moderate, serious, and critical

Effects of interventions—health services utilization

Four RCTs reported HSU as secondary outcomes [17, 38, 39, 43]. Three of these studies reported ED visits [17, 39, 43], three reported hospitalizations [17, 38, 43], and two reported unscheduled clinic visits [39, 43]. Two studies had reactive interventions [17, 43], and two had scheduled interventions [38, 39]. One study reported HSU as combined outcome (clinic and ED visits) [39]. Yount et al. were the only study to report total number of ED visits, hospital admission, and unscheduled clinic visits separately [43]. A meta-analysis was not able to be performed due to significant heterogeneity in reported outcome measures including composite outcomes and differences in how outcomes were measured.

Compared to usual care, no studies reported a significant improvement in the telehealth intervention groups. Basch et al. found no significant difference between the cumulative incidence of patients who visited the ED (p = 0.16) or were hospitalized (p = 0.75) over a 1-year period for those exposed to reactive telehealth [17]. Over the 12-week study period, Yount et al. reported no statistically significant difference in HSU (ED visits: p = 0.848, hospitalizations: p = 0.877, unscheduled clinic visits: p = 0.129) for those exposed to reactive telehealth [43]. Bouleftour et al. reported the proportion of hospitalized patients who received scheduled telehealth appeared lower at 6, 12, and 24 weeks; these differences were not significant, including at 12 weeks when the difference was most pronounced (p = 0.077) [38]. Cirillo et al. did not find any significant difference in the overall number of patients with at least one ED or unscheduled oncology clinic visit, or visits judged to be unavoidable, after two cycles of chemotherapy for those exposed to scheduled telehealth [39].

Effects of interventions—quality of life

Seven studies assessed QOL [14, 17, 23, 38, 40, 41, 43]. Two studies used the EuroQol EQ-5D [17, 38], two used the Functional Assessment of Cancer Therapy-General (FACT-G) [23, 43], and one each used the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30) [41], Functional Living Index-Cancer (FLIC) [40], and the Pediatric Quality of Life Inventory 4.0 (PedsQL 4.0) [14]. Four studies assessed reactive telehealth [14, 17, 41, 43] and three evaluated scheduled telehealth [23, 38, 40].

For the RCTs, there was no significant difference between the intervention and control groups for improving QOL (SMD 0.10; 95% CI − 0.13, 0.34; 4 studies) (Fig. 4: Analysis 1.1) [17, 23, 41, 43]. CBA trials showed no significant difference in post-intervention QOL scores (SMD − 0.02; 95% CI − 0.79, 0.75; 2 studies) [14, 40]. There was significant clinical and statistical heterogeneity (I² = 63% for RCTs, 80% for CBA studies). The certainty of findings is very low according to GRADE.

Fig. 4.

Meta-analyses: Telehealth versus usual care

Subgroup analysis by intervention type (reactive and scheduled) did not show a significant change in QOL post-intervention scores in RCTs (SMD 0.15; 95% CI − 0.12, 0.42; 3 reactive studies) (Fig. 4: Analysis 1.2) [17, 41, 43]. In a sensitivity analysis, the effect estimate was similar when Kornblith et al. [41] were removed due to high risk of bias for incomplete outcome data. There remained no statistical difference between intervention and control groups.

Effects of interventions—symptom severity

Nine studies (7 RCTs, 2 CBA) reported severity of symptoms as an outcome [11, 14, 23, 38–43]. Two studies used the National Cancer Institute Common Toxicity Criteria for Adverse Events (NCI CTCAE v4.0) [38, 39], and other studies used the following: Hospital Anxiety and Depression Scale (HADS) [41]; Chemotherapy Symptom Assessment Scale (CSAS) [23]; a numeric severity scale [11]; Memorial Symptom Assessment Scale-Short Form (MSAS-SF) [42]; Patient Health Questionnaire-4 (PHQ-4) [42]; FACT-Lung Symptom Index (FLSI) [43]; Edmonton Symptom Assessment Scale (ESAS) [40]; Brief Pain Inventory (BPI) [14].

Four studies (2 RCTs and 2 CBA) reported post-intervention individual symptom severity scores [14, 23, 40, 41]. Pain was the only symptom with enough data to perform a meta-analysis and was significantly reduced by the telehealth interventions (SMD − 0.54; 95% CI − 0.88, − 0.19) in two CBA studies [14, 40] (Fig. 4: Analysis 1.3). There was no statistically significant heterogeneity (I² = 0); however, clinically these studies had small sample sizes (40 [14] and 80 [40] participants), assessed very different populations (adolescents [14] vs adults [40]), and had very different interventions (twice daily assessment with a smartphone application (reactive intervention) [14] vs phone calls within the first week after each chemotherapy session (scheduled intervention) [40]). The certainty of findings is very low according to GRADE.

Four studies that evaluated differences between groups found significant symptom reduction (reactive [11, 41], scheduled [23, 40]). In a multicenter trial of patients beginning chemotherapy, Mooney et al. found that intervention participants who self-reported symptoms daily through a telephone voice reporting system and received a reactive call by the NP if symptoms exceeded pre-set thresholds had less symptom severity across all symptoms and lower mean symptom scores for fatigue, pain, sleep problems, nausea/vomiting, depression, anxiety, neuropathy, and sore mouth (p < 0.05) throughout the trial compared to controls [11]. Kornblith et al. reported significantly less anxiety (p < 0.0001) and depression (p < 0.0001) in older patients who received reactive telephone calls if their monthly reported symptom scores exceeded a threshold while receiving cancer treatments in addition to written educational materials, compared to those who just received educational materials [41]. Lai et al. found a significant reduction in 4 of 22 symptoms (mouth/throat problems, fatigue, neuropathy, distressful feelings) assessed during their trial of breast cancer patients receiving adjuvant chemotherapy who received pre-chemotherapy nurse consultation and scheduled nurse telephone calls (within 1 week after the first, second, fourth, and sixth cycles) [23]. Hintistan et al. found symptom severity to be significantly reduced across all domains (p < 0.05: pain, fatigue, nausea, anxiety, anorexia, dyspnea, skin and nail changes, mouth sores, neuropathy) in the intervention group who received scheduled nurse telephone calls within the first week after each chemotherapy session (6 calls), compared to the control group [40].

Asthenia and pain were the most common symptoms in 92 patients who received 15 scheduled nurse telephone calls; however, Bouleftour et al. did not report on severity [38]. In a study of patients receiving oral anticancer treatments, Cirillo et al. did not report any significant difference in the number of participants with symptoms of severe toxicity who received scheduled nurse telephone calls (days 7 and 14 of cycle 1, and day 14 of cycle 2 of chemotherapy) [39]. Traeger et al. found no significant differences in the number of participants in each group having elevated depression or anxiety symptoms at mid- or post-intervention assessments for patients with lung, colorectal, or breast cancer receiving two scheduled telephone calls from an oncology NP during the first week of each of their first two chemotherapy cycles [42].

Discussion

Our systematic review focused on nurse-led telehealth interventions for symptom management in patients with cancer receiving systemic or radiation therapy. Eight RCTs and two quasi-experimental studies met eligibility criteria, assessing 2315 participants [11, 14, 17, 23, 38–43]. There were an equal number of studies assessing reactive and scheduled interventions. Individual studies found telehealth interventions were associated with improved QOL and reduction in symptom severity but did not reduce HSU compared to usual care. Meta-analyses, including subgroup analysis, did not reveal any significant difference in QOL scores. Two CBA studies (1 reactive, 1 scheduled) showed significant reduction in pain severity in telehealth intervention groups. Our findings lead to the following points for discussion.

Telephone-based telehealth services were the most common mode of delivery in the included studies. This was not unexpected as it is commonly used by nurses to aid in symptom management [11, 23, 38–44]. Despite the increase in diversity of telehealth modalities, only two studies evaluated the use of web-based services [14, 17] for symptom monitoring.

Given rising healthcare costs, determining which interventions can lower unnecessary HSU is critical. Despite this, there is limited evidence on how the use of telehealth will impact healthcare costs [29, 45]. The four included studies that measured HSU showed no significant differences between telehealth interventions and usual care [17, 38, 39, 43]. However, there was significant heterogeneity in the included studies with respect to the patient populations, type of intervention, frequency of delivery, and outcomes measured which prevented meta-analysis. These findings are consistent with previous reports that tele-oncology provided no additional HSU benefits compared to in-person services [46].

Many previous reviews have also found methodological limitations and heterogeneity issues when attempting to determine if telehealth would be a beneficial intervention to incorporate into practice [27, 29, 30, 47]. For exclusively internet-based interventions, Moradian et al. concluded that the methodological limitations hindered analysis and called for improved quality research [30]. The lack of significant findings may also be impacted by our measures of HSU which did not include hospital length of stay or direct healthcare costs, both of which could be influenced by telehealth interventions. This is particularly relevant as most studies in our review reported reduced symptom severity for telehealth compared to usual care [11, 14, 23, 40, 41], which may result in shorter hospital admissions and reduced direct healthcare costs. Future studies should consider a more inclusive list of costs when implementing telehealth interventions, particularly in comparison to the costs of providing the telehealth intervention itself.

Telehealth is previously known to reduce the time to access healthcare services, and intervening at the earliest time may provide the best opportunity to see improved QOL [48–52]. Swift intervention is more consistent with the reactive mode of telehealth, as it regularly captures self-reported symptom severity from patients, triggering an alert to their healthcare team who can help with symptom management. In contrast, pre-scheduled symptom monitoring may allow for more frequent contact with patients, but patients may experience a worsening of symptoms between contacts, which could lead to less timely access to care. Despite this, subgroup analysis did not reveal a significant difference in the QOL in either reactive or scheduled intervention studies. This finding may be due to small number of included studies and future research into most effective timing of intervention may be beneficial.

Previous research has shown that patients with complexities, due to chronic conditions, may have improved QOL when using web-based interventions [30, 53]. Two web-based studies included reported improved QOL [14, 17]. One of these studies focused on metastatic patients [17], which adds to the evidence that regularly monitoring symptom severity through web-based applications may be more beneficial in patients with advanced disease and more severe symptoms.

Our review found both reactive and scheduled telehealth studies, which reported reduced severity of symptoms in the intervention group compared to controls. Our findings on reduced symptom severity were similar to other reviews. A systematic review by Moradian et al. found four of six studies reported a reduction in the severity of symptoms for participants receiving internet-based interventions for managing chemotherapy-related symptoms in patients with cancer [30]. Ream et al.’s systematic review of 32 studies found that telephone-delivered interventions for symptom management in adults with cancer were effective for symptoms such as depression, anxiety, fatigue, and emotional distress [27]. In the systematic review of 20 studies by Chen et al., telehealth interventions improved quality of life, self-efficacy and depression, distress, and perceived stress in patients with breast cancer [47]. Previous reviews did not compare reactive to scheduled interventions, or specifically assess nurse-led interventions. The results of this review are consistent with previous systematic reviews in this area which reported limited availability of studies, methodological limitations, and heterogeneity [27, 29, 30, 47].

This review focused on nurse-led telehealth interventions for symptom management and did not include studies which assessed post-treatment follow-up programs [29], education programs [27, 47], psychological interventions [27, 47], or patient’s carers or partners [27] which were included in other reviews. The implementation of these additional programs/interventions may provide additional benefits but may also be more costly, requiring additional expertise that may not be widely available within ambulatory oncology centers. For example, the degree of training and expertise influences the success of telehealth symptom management programs. Providing training workshops for nurses on the use of evidence-informed practice guides for telephone-based symptom support has been shown to improve nurses’ confidence in providing symptom support and using the practice guides [54]. However in this review, the descriptions of educational preparation of nurses providing telehealth services were variable across studies and it was impossible to determine the influence of their educational preparation on the outcomes of the telehealth interventions.

Strengths and limitations of review

A strength of this review was the high methodological quality. According to AMSTAR II, this review met 15 of 16 items [55]. The missing item was not investigating for publication bias. Although this review allowed for greater variety of telehealth interventions and cancer types not previously included in other reviews, there are some limitations that should be considered when interpreting the findings. There was heterogeneity due to differences in the intervention design, populations, and outcome reporting that interfered with our ability to combine findings across studies. Limiting inclusion to nurse-led telehealth interventions missed studies of telehealth interventions provided by other healthcare professionals. This review focused on HSU as a surrogate for health system costs but did not directly assess costs.

Conclusion

Patients with cancer undergoing systemic and radiation therapies may develop symptoms that result in visits to the ED or hospitalization. This review focused on nurse-led telehealth interventions for symptom management in patients with cancer as a possible method of reducing HSU. Although it did not find any evidence that telehealth interventions reduced HSU or improved QOL, there was some evidence for decreased severity of symptoms from both reactive and scheduled telehealth interventions. Synthesizing findings across studies is limited due to significant heterogeneity in the telehealth interventions, participants, and outcomes measured. Future research can improve the quality of evidence in this area by evaluating interventions more consistent with current practice for patients receiving cancer treatments and providing more consistent reporting of outcomes.

Supplementary information.

Supplementary Information

Below is the link to the electronic supplementary material.

Author contribution

All authors contributed to the study conception and design. Search strategy and analysis was performed by CK. Study screening, data extraction, and preparing the first draft of the manuscript were performed by CK, CD, and NM. All the co-authors listed contributed to reviewing and revising the manuscript and have approved it for submission. The protocol was not registered but is available upon request.

Data availability

Not applicable.

Code availability

Not applicable.

Declarations

Ethics approval

This is a systematic review and meta-analysis; ethics approval is not required.

Consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.