| Eight studies—four Level 1B and four Level 2B—that examined the use of multimodal sensory stimulation met the criteria for inclusion, providing moderate strength of evidence to support this type of intervention. |
Bahonar et al. (2019)
Level 1B—RCT
Setting
Intensive care
Country
Iran |
Population
Adults with disorders of consciousness following TBI in intensive care units. N = 120
Intervention
Group A received auditory stimulation (nature sounds). Group B received tactile stimulation (foot sole reflexology). Group C received auditory (nature sounds) and tactile (foot reflexology) stimulation. Group D: Control received only routine care.
Delivery Method
Researcher delivered intervention to participants individually.
Dose
30 min, twice a day, every day for 2 wk (all intervention groups). |
Significantly fewer days to regain consciousness were recorded in foot reflexology and nature sounds + foot reflexology compared with control group (p = .001). |
Megha et al. (2013)
Level 2B—RCT
Setting
Intensive care
Country
India |
Population
Adults with disorders of consciousness following TBI in intensive care unit. N = 30
Intervention
Groups A and B received multimodal coma stimulation including visual, auditory, olfactory, tactile, and gustatory. Group C (control group) received usual physiotherapy care (e.g., positioning, stretching and passive movements).
Delivery Method
Participants received the intervention individually by either a therapist or family member.
Dose
Group A (high frequency)—five 20-min sessions per day for 5 consecutive weekdays for 2 wk. Group B (low frequency)—two 50-min sessions per day for 5 consecutive weekdays for 2 wk. Group C—physiotherapy was provided twice daily for 5 consecutive weekdays for 2 wk. |
There was a significant difference between Groups A and C and B and C for both the GCS and Western Neuro Sensory Stimulation Profile assessments indicating that multimodal coma stimulation is effective compared with the control group. |
Salmani et al. (2017)
Level 1B—RCT
Setting
Trauma care unit
Country
Iran |
Population
Adults with disorders of consciousness following TBI in a trauma care unit. N = 90
Intervention
Group A: Family member with strongest emotional relationship with patient was trained in family-centered affective stimulation. Affective stimulation including auditory stimulation for 20 min, sensory stimulation for 10 min, kinetic stimulation for 15 min, and affective conversation. Group B (Placebo): A trained person unfamiliar to all patients in placebo group provided them with purse sensory stimulation (auditory, tactile, and kinetic) and communicated about services, treatments, and health status. Group C (Control): Received usual care services and sensory stimulation that is routinely provided (e.g., adjustments of lighting, equipment noise). Physical care services were also provided to Groups A and B. Family visitation occurred through a room window in accordance with rules and regulations.
Delivery Method
Participants were treated individually. Group A (Intervention): Visitation by family member. Group B (Placebo): Visitation by a trained, nonfamiliar person. Group C (Control): Visitation according to routine procedures.
Dose
Groups A and B: 30- to 45-min sessions, twice a day for 7 days. |
Improvement in the intervention group’s level of consciousness was significantly greater than the control and the placebo groups. Recovery rate and effect sizes confirmed the greater effectiveness of the intervention group (family-centered affective sensory stimulation) compared with placebo (pure sensory stimulation). |
Sato et al. (2017)
Level 2B—Single group pre–post
Setting
Nursing home care
Country
Japan |
Population
Adults with disorders of consciousness following TBI in a persistent vegetative state. N = 21
Intervention
Participants were positioned upright in bed without back support for 3 min the first week and upright sitting with feet placed on the floor for 5–8 min during Wk 2 and 3. Participants also received a footbath (10 min) with massage (5 min). Participants also received oral care for 30 min each day. A control group of six conscious patients who are bedridden also received these interventions.
Delivery Method
Stimuli provided to each participant individually by nursing.
Dose
All interventions (positioning, footbath, and oral care) were conducted from 0900 to 1100 every day for 3 wk. |
The intervention was found to improve the patients’ levels of consciousness statistically significantly. |
Kalani et al. (2016)
Level 1B—RCT
Setting
Intensive care unit
Country
Iran |
Population
Adults with disorders of consciousness following TBI. N = 64
Intervention
Group A (Intervention Group): received orientation, music, reading of prayers or poems, playing recordings of familiar voices, joint mobilization, and application of lotion to hands and feet. Group B (Control Group): received family visits.
Delivery Method
All participants received individual interventions. In Group A (Intervention Group) the family delivered the treatment. In Group B (Control Group) the family was able to visit their loved one for 30 min.
Dose
Group A (Intervention Group)—sessions were for 45–60 min daily for 2 wk. Group B (Control Group)—family had visiting hours for 30 min thrice a week for 2 wk. |
After 2 wk, the level of consciousness improved in the intervention and control groups, but the increase in the intervention group was significantly more than the control group. |
Cheng et al. (2018)
Level 2B—ABAB Withdrawal Design
Setting
Rehabilitation
Country
China and Italy |
Population
Adults with disorders of consciousness following TBI at least 1 mo postinjury. N = 29
Intervention
SSP included visual stimulation, auditory stimulation, tactile stimulation, olfactory stimulation, and gustatory stimulation.
Delivery Method
Participant received both the intervention and control phases individually. Each phase lasted 4 wk. During the intervention phase, participants were administered the SSP.
Dose
SSP was administered twice a day for three days each week. Each stimulation was applied three times on both sides of the patient and lasted approximately 20 min each session. |
There was a significant difference between treatment phases, where participants in the minimally conscious state had higher CRS-R total scores (medium effect size), and no treatment phases (control). |
Moattari et al. (2016)
Level 2B—RCT
Setting
Intensive care unit
Country
Iran |
Population
Adults with disorders of consciousness following TBI at least three days postinjury. N = 60
Intervention
SSP included five parts: 1) awakening for 5 min, 2) auditory stimulation for 10 min (favorite music or taped recordings of family members), 3) visual stimulation for 10 min (familiar object, family photograph, film, etc.), 4) tactile stimulation for 5 min, and 5) olfactory stimulation for 10 s (favorite aromas).
Delivery Method
All participants received individual interventions. Participants randomized to one of three groups. In Group A, the nurse delivered the sensory stimulation program. In Group B, a family member delivered the sensory stimulation program. In Group C, participants received usual care (control).
Dose
Groups A and B received the SSP for 30-min intervals, 2×/day for 7 days. |
Both intervention groups improved; however, SSP administered by family demonstrated significantly higher scores on the GCS (p = .001), Rancho Los Amigos (p = .001), Western Neurosensory Stimulation Profile (p = .001) after 7 days compared with the other two groups. |
Chuaykarn & Jitpanya (2017)
Level 1B—RCT
Setting
Surgical wards in a hospital
Country
Thailand |
Population
Adults with disorders of consciousness following TBI at least three days postinjury. N = 45
Intervention
Group A (4 senses) received auditory, visual, tactile, and kinesthetic stimulation. Group B (5 senses) received auditory, visual, tactile, olfactory, and gustatory stimulation. Group C (control) received usual care.
Delivery Method
All participants in the intervention groups were provided stimuli individually. Participant sat upright in bed. Stimuli provided by a researcher who oriented the participant to date, time, place, reason for being in the hospital, and also explained what they were about to do.
Dose
Group A—sessions were for 30 min, twice a day, every day for 2 wk. Group B—sessions were 15-30 min, five times a day, every day for 2 wk. |
Significantly better CRS-R scores were obtained in both intervention groups compared with control beginning on day 7 and continuing through day 14 (p < .001). |
| Three studies—two Level 1B and one Level 2B—that examined the use of unimodal auditory stimulation focusing on familiar voices telling structured familiar stories were included. Moderate strength of evidence supports this type of intervention. |
Mohammadi et al. (2019)
Level 1B—RCT
Setting
Intensive care unit
Country
Iran |
Population
Adults with DoC following TBI within 72 hr postinjury. N = 60
Intervention
The family member closest to the patient recorded a 10-min message. Recording of family members message occurred in ICU visitation room and included the information about time and place (30 s), the accident which included head trauma (30 s), a shared sweet memory (4 min), and promising and encouraging words about the patient’s recovery and future (5 min).
Delivery Method
All participants in the intervention group were provided stimuli individually. Participants were randomized to either an intervention or control group.
Dose
10 min played in the afternoon for 3 consecutive days. |
A significant increase in level of consciousness was found in the intervention group and not the control group. |
Parveen et al. (2015)
Level 1B—RCT
Setting
Neurosurgery wards
Country
India |
Population
Adults with disorders of consciousness following TBI within 72 hr postinjury. N = 80
Intervention
Script included present condition of illness, patient-related events, and information about family members, colleagues, home, and workplace. Family approached patient by calling the patient’s name, introducing themselves and then talk using prewritten script in a way that it brings hope and a feeling of worthiness in the patients. Termination of script occurred by providing information regarding next visit by the family.
Delivery Method
Participants were randomized to an intervention or control group. All participants in the intervention group were provided stimuli individually.
Dose
8–10 min per session, twice a day for 2 wk. |
Total GCS and motor score in intervention group was significantly higher by day 7 compared with control group. |
Pape et al., (2015)
Level 2B—RCT
Setting
Acute inpatient research bed
Country
USA |
Population
Adults with disorders of consciousness following TBI between 28 days to 1-yr postinjury. N = 15
Intervention
FAST includes customized recordings of stories told by people well known to the patient. Stories represent specific events experienced by both the participant and storyteller. Control Group received placebo of silence.
Delivery Method
Participants were randomized to an intervention or control group. All participants were provided stimuli individually via compact discs.
Dose
10 min, 4 times per day, with at least 2 hr in between for 6 wk (intervention and control). |
Participants with FAST intervention compared with control group demonstrated statistically significant improvement on the Coma Near Coma Scale. |
| One Level 2B study examined the use of unimodal auditory stimulation that uses familiar voices telling unstructured content. Low strength of evidence supports this type of intervention. |
Park & Davis (2016)
Level 2B—Crossover design
Setting
Hospital
Country
Not stated |
Population
Adults with DoC following TBI within 3 wk postinjury. N = 9
Intervention
Direct auditory stimulation included voices of family and familiar music. Nondirect auditory stimulation included less interactive sounds via TV of music type sounds.
Delivery Method
All participants were provided auditory stimuli individually.
Dose
Participants received both direct and nondirect auditory stimulation in randomized order. After either direct or nondirect auditory stimulation there was a washout period of one hour. 15 min for each stimulation session, 5–8 sessions per day for 3–5 days. |
Both direct and indirect stimulations demonstrated increases on the GCS and SSAM. SSAM captured statistically significantly greater improvement after direct auditory stimulation compared with indirect auditory stimulation. |
| One Level 1B study examined the use of unimodal auditory stimulation that focuses on familiar music. Low strength of evidence supports this intervention. |
Rahimi, Salehi, & Seidi (2019)
Level 1B—RCT
Setting
Intensive care unit
Country
Iran |
Population
Adults with DoC following TBI with stable vital signs after being in the intensive care unit for 24 hr. N = 70
Intervention
Pleasant acoustic stimuli was played for the patient using headphones. The pleasant audio stimuli (e.g., voices of family members, favorite music) were selected by the patient’s family based on the patient’s interests. Acoustic stimuli were approved by the family and physician. Control group listened to silence.
Delivery Method
Participants were randomized to an intervention or control group. All participants were provided auditory stimuli individually via headphones.
Dose
10 min between 3 to 6 p.m., once a day for 7 days. |
After day 3, all GCS scores significantly improved in the intervention group compared with the control group. |
| One Level 2B study examined the use of unimodal auditory stimulation that focuses on verbal orientation. Low strength of evidence supports this intervention. |
Hoseinzadeh et al. (2017)
Level 2B—RCT
Setting
Intensive care unit
Country
Iran |
Population
Adults with DoC following TBI with stable vital signs after being in the intensive care unit for 3 days. N = 40
Intervention
The nurse gathered organized auditory stimulation information from the patients’ relatives. Content included the place, time and date, patient identification factors (e.g., age), details of family members and some occupational information. Information was recorded by a male nurse.
Delivery Method
Participants were randomized to an intervention or control group. All participants receiving the intervention were provided auditory stimuli individually via headphones.
Dose
10 min for 10 days—morning, afternoon, and before 10 o’clock at night. |
Significant improvement was found as assessed by the GCS for the intervention group compared with the control group on day 10. |