| Literature DB >> 23935572 |
Susy Braun1, Melanie Kleynen, Tessa van Heel, Nena Kruithof, Derick Wade, Anna Beurskens.
Abstract
OBJECTIVE: To investigate the beneficial and adverse effects of a mental practice intervention on activities, cognition, and emotion in patients after stroke, patients with Parkinson's disease or multiple sclerosis.Entities:
Keywords: mental practice; meta-analysis; neurorehabilitation; systematic review
Year: 2013 PMID: 23935572 PMCID: PMC3731552 DOI: 10.3389/fnhum.2013.00390
Source DB: PubMed Journal: Front Hum Neurosci ISSN: 1662-5161 Impact factor: 3.169
Figure 1Overview of literature search. Abbreviations: MP, mental practice; PD, Parkinson's disease; MS, multiple sclerosis; RCTs, randomized controlled trials.
Amsterdam-Maastricht Consensus List for quality assessment rating criteria.
| (1A) Randomization | Item has a positive score if the concealment of treatment allocation is explicitly described to be randomized (e.g., computer generated block randomization) |
| Note: Quasi-randomization is scored negative (e.g., randomization of dates of birth or day of the week) | |
| (1B) Concealment of allocation | Item has a positive score if explicitly is described that the allocation of the intervention was blinded (e.g., a independent assessor performs the allocation and has no information/influence on who will be allocated to which group) |
| (2) Comparable sub groups at baseline | Item has a positive score if the study groups are comparable at baseline with the most important prognostic factors (e.g., comparable mean age and standard deviation in the study groups) |
| (3) Blinded care provider | Item has a positive score if the care provider is blinded regarding treatment allocation (e.g., the care provider is unaware of the content of the intervention |
| (4) Correction for attention; same treatment (dose), co-intervention | Item has a positive score if the different intervention groups have the same treatment dose and if co-interventions are equally divided among the intervention groups. Also, participants in both groups are asked to provide the same information (e.g., fill in logs) and undergo the same tests (battery) |
| (5) Acceptable compliance | Item has a positive score if participants themselves or therapist and relatives report that the participants followed the given instructions (e.g., through logs, interviews) |
| (6) Blinded patient | Item has a positive score if patients are blinded regarding treatment allocation and if the method of blinding is appropriate (e.g., the patient is unaware of the treatment content |
| (7) Acceptable withdrawals during intervention period | Item has a positive score if the percentage of patients that drop out of the study does not exceed 10% during the intervention period. Another 10% of loss to follow-up of the remaining sample is set as acceptable for the follow-up period |
| (8) Blinded outcome assessor | Item has a positive score if the outcome assessors are blinded regarding treatment allocation (e.g., independent raters, who are unaware of the treatment group that the participant is in–preferably checked by asking the rater to predict who is in which group) |
| (9) Relevance measures | Item has a positive score if the measurement instruments allow answering the research question |
| (10) Timing assessment | Item has a positive score if the outcome assessment takes place approximately at the same time in all intervention groups. Also, a follow-up period of at least 3 months is set to be acceptable |
| (11) Intention to treat analysis | Item has a positive score if all randomized patients are reported for all measuring points and are analysed according to the group they were originally randomized to |
Blinding of the care provider and of the patient is not always applicable in physical therapy because of the nature of physical therapy interventions (e.g., manual therapy, exercises). Proper double blinding, therefore, is unlikely to be accomplished for most physical therapy trials (Olivo et al., .
Quality assessment of internal validity of the RCTs with the AMCL: stroke and Parkinson's disease (PD) population.
Each criterion was scored either positive (+, 1 point), negative (–, 0 points), or unclear (?, 0 points). If the score changed after additional information from the authors or earlier confirmed data from other reviews were retrieved, then the initial score from the independent reviewers is shown between brackets.
A maximum score of 11 points per study could be achieved (1 point for the items 2–11; ½point for the items 1a and 1b).
The last row of the table shows the total score on the AMCL for all 16 included studies. The top number is the score after additional information from the authors or earlier confirmed data from other publications had been processed. The lower row shows the scores based on information from the original articles only.
Overview of study characteristics of included RCTs: stroke and Parkinson's disease population.
| Page et al., | Randomized controlled trial | Primary outcome and primary outcome measure:
- ARAT and FM | MP added to therapy may have effects on selectivity and ability of the arm and hand | Interviews and logs were used but showed no side-effects or effects on cognition/emotion | |
| N total: 13 | Both groups:
- 6 wk intervention period, 3×/wk 60 min - 30 min upper limb and 30 min lower limb | Timing:
- Pretest, posttest 6 wk after the start of the intervention - No follow-up | No test for significance was performed | ||
| N (EG): 8 | |||||
| N (CG): 5 | |||||
| Mean age, SD (years): Total: 64.6 ± 14.6 | Experimental group:
- Daily imagery by tape; 3×/week at home, 2×/week in the clinic - Content tape: 2–3 min relaxation, 7 min MP of ADLs, 2 min refocusing - Three different scripts, 1 for every 2 wk (reaching for and grasping a cup or object, turning a page in a book, proper use of a pencil or pen) - Kinesthetic and visual imagery | ||||
| Time post-stroke (months):
EG: range: 2–11 CG: range: 3–11 | |||||
| Control group:
Tape: 10 min; information about stroke (both at home and in the clinic) | |||||
| Liu et al., | Prospective randomized controlled trial | Primary outcome and primary outcome measure:
- Patient performance on tasks using a 7-point Likert Scale (trained and untrained tasks) | MP might improve the execution of both trained and untrained tasks | MP group showed significantly greater improvement CTT (subscale) score across time than control group, possibly indicating increased attention and sequential processing | |
| N total: 46 | Both groups:
- 3 wk 5×/week for 60 min: PT - 3 wk intervention period, 5×/wk for 60 min with either experimental or control intervention by an OT - Tasks: 15 trained functional tasks including household, cooking and shopping tasks, standardized for all patients of the experimental group - First week easy tasks such as laundry folding, third week: shopping, taking transportation | Secondary outcome and secondary outcome measure:
- FM - CTT | |||
| N (EG): 26 | |||||
| N (CG): 20 | |||||
| Mean age, SD (years):
EG: 71.0 ± 6.0 CG: 72.7 ± 9.4 | |||||
| Mean time post-stroke, SD (days):
EG: 12.3 ± 5.3 CG: 15.4 ± 12.2 | Experimental group:
- Daily imagery - First week: analyzing task sequences (motor planning) - Second week: problem identification through MI - Third week: practicing - Kinaesthetic and visual imagery was used | Timing:
- Pre-test, post-test 3 wk after the start of the intervention - Follow-up 1 month after post-test | |||
| Control group:
- Daily OT conventional functional retraining program - Same dose as intervention MP | |||||
| Page et al., | Randomized controlled trial | Primary outcome and primary outcome measure:
- MAL - ARAT | MP added to therapy as usual may have effects on the use and ability of the arm and hand | – | |
| N total: 11 | Both groups:
- 6 wk intervention period, 2×/wk 30 min OT apart from intervention - Task: functional movements of ADLs using affected arm, standardized for all patients of the experimental group | ||||
| N (EG): 6 | |||||
| N (CG): 5 | |||||
| Mean age, SD (years):
Total: 62.3 ± 5.1 | Experimental group:
- MP by tape after physical practice for 30 min: 5 min relaxation, 20 min MP, 3–5 min refocusing - Internal, cognitive polysensore images were suggested | Timing:
- Twice a pre- and once a posttest 6 wk after star of the intervention - No follow-up | |||
| Mean time post-stroke (months):
N total: 23.8 (range: 15–48) | Control group:
- Tape: 30 min; progressive relaxation (Jacobson) | ||||
| Page et al., | Randomized placebo-controlled trial | Primary outcome and primary outcome measure:
- FM (upper extremity) - ARAT | MP added to therapy as usual may have effects on selectivity and ability of the arm and hand | – | |
| N total: 32 | Both groups:
- 6 wk intervention period, 2×/wk 30 min physical therapy apart from MP - Task: functional movements of ADL using affected arm - Three versions: 1 for every 2 wk | ||||
| N (EG): 16 | |||||
| N (CG): 16 | |||||
| Mean age, SD (years):
EG: 58.69 ± 12.86 CG: 60.38 ± 14.17 | Experimental group:
- MP by tape: 5 min relaxation, 20 min MP, 3–5 min refocusing - Internal, cognitive polysensore images were suggested - 1st person view - Kinaesthetic and visual imagery were used | Timing
- Pre-test twice, post-test 1 wk 6 wk after the start of the intervention - No follow-up | |||
| Mean time post-stroke, SD (months):
EG: 38.81 ± 25.86 CG: 45.19 ± 43.56 | Control group:
- Tape: 30 min; progressive relaxation (Jacobson) | ||||
| Muller et al., | Pre-set randomized controlled trial | Primary outcome and primary outcome measure:
- Jebsen Test (slope differences) - Pinch Grip (slope differences) | No differences between the two experimental groups (MOTOR and MENTAL) | - | |
| All groups:
- 4 wk intervention period, 5×/wk 30 min therapy | |||||
| N total: 17 | Experimental group1: MENTAL
- First session: video-taped finger movement sequence: execute movement until correct order was completed - Thereafter: short refreshment by video followed by only mental rehearsals - Kinaesthetic and visual imagery were used | Timing
- 2-week pre-testing - 1-week post-testing 4 wk after the start of the intervention - No follow-up | - Improvement within both experimental groups on all subscales for upper limb use. - Significant differences between both the MOTOR and MENTAL groups on the one hand and the control group on the other in pinch grip and two subscales of the Jebsen Test (“writing” and “simulated feeding”) | ||
| N (EG1): 6 | |||||
| N (EG2): 6 | |||||
| N (CG): 5 | |||||
| Mean age, SD (years):
N total: 62 ± 10 | Experimental group2: MOTOR
- Perform training task with the affected hand | ||||
| Mean time post-stroke, SD (days):
Total: 28.7 ± 21.2 | Control group:
- Physical therapy | ||||
| Liu et al., | Randomized controlled trial | Primary outcome measure:
- Performance gains; measuring instrument not mentioned (NRS or Likert Scale) | MP had effect on most of the complex tasks trained:
- In 4/5 trained tasks in familiar environment - In 3/5 trained and 2/3 untrained tasks in novel environment | Patients in the MP group seemed to be more able to form cognitive mapping of routes and plan actions in unfamiliar surroundings (effects on cognition) | |
| N total: 35 | Both groups:
- 3 wk 5×/week for 60 min: PT - 3 wk intervention period, 5×/wk for 60 min with either experimental or control intervention by an OT - Tasks: 15 trained functional tasks including household, cooking and shopping tasks, standardized for all patients of the experimental group - Each wk, 5 tasks with similar level of difficulty were covered, progressing from the easiest to the most difficult | ||||
| N (EG): 18 | |||||
| N (CG): 17 | |||||
| Mean age, SD (years)
EG: 70.8 ± 9.3 CG: 69.7 ± 7.4 | Timing:
- Pre-test, post-test 3 wk after the start of the intervention - No follow-up | ||||
| Mean time post-stroke, SD (days):
EG: 12.2 ± 5.1 CG: 12.3 ± 7.4 | Experimental group:
- MP; 5×/wk 60 min - MP involved patients truncating, self-reflecting, feedback, mentally rehearsing combined with performing the activity - Kinaesthetic and visual imagery were used | MP might improve the execution of both trained and untrained tasks | |||
| Control group:
- Control for attention; 5×/wk 60 min (same dose as MP) - Use of a demonstration-then-practice method | |||||
| Liu, | Single-blind randomized controlled trial | Primary outcome measure:
- 7-point Likert scale | MP had effect on most of the complex tasks trained:
- In 3/5 trained tasks in primary outcome measures in familiar environment - in 5/5 trained tasks in novel environment | No differences between groups were measured with the Cognistat | |
| N total: 34 | Both groups:
- 3 wk daily PT for 60 min - 3 wk intervention period, 5×/wk for 60 min with either experimental or control intervention by an OT - Tasks: 15 trained functional tasks including household, cooking and shopping tasks, standardized for all patients of the experimental group - Each wk, 5 tasks with similar level of difficulty were covered, progressing from the easiest to the most difficult | Secondary outcome and secondary outcome measure:
- FM - Cognistat | |||
| N (EG): 17 | |||||
| N (CG): 17 | |||||
| Mean age, SD (years):
EG: 70.4 ± 9.8 CG: 68.1 ± 10.5 | Timing:
- Pre-test, post-test 3 wk after the start of the intervention - No follow-up | Patients in the MP group seemed to be more able to form cognitive mapping of routes and plan actions in unfamiliar surroundings (effects on cognition) | |||
| Mean time post-stroke, SD (days):
EG: 12.3 ± 5.3 CG: 12.3 ± 7.4 | Experimental group:
- MP: 5×/wk 60 min of which 30 min actually performing the task - MP (30 min) involved self-reflecting and mental imaging - Kinaesthetic and visual imagery were used | MP improved the execution of both trained and untrained tasks. This might indicate that patients in the experimental group were able to generalize learned skills to new situations better than the control group | |||
| Control group:
- Control for attention: 5×/week for 60 min (same dose) - Use of a demonstration-then-practice method | |||||
| Page et al., | Randomized controlled trial | Primary outcome measure:
- ARAT - FM (upper extremity) | Larger score changes on the ARAT and FM in the experimental group compared to the control | - | |
| N total: 10 | Both groups:
- 10 wk intervention period - Modified constrained-induced therapy (5 h/day, 5 days/wk) - 3 days/wk, 30 min therapy (functional activities) | Timing:
- Pre-test twice, post-test 11 wk after the start of the intervention - Follow-up 3 months after the start of the intervention | Differences between groups in favor of the experimental group at post-test but not at follow-up on both the ARAT as FM | ||
| N (EG): 5 | |||||
| N (CG): 5 | |||||
| Mean age (years):
EG: 58.4 (range: 48–72) CG: 64.4 (range: 56–79) | Experimental group:
- MP: 10 wk, directly after therapy (3×/wk 30 min) by tape - 5 different tapes (each for 2 wk) with activities of daily living (practiced in therapy) - Homework: daily cognitive rehearsal - Visual and/or kinaesthetic imagery (patients' preference) was used | No test for significance was performed | |||
| Mean time post stroke (months):
EG: 26.4 (range: 13–45) CG: 30.6 (range: 17–42) | Control group:
- Therapy as usual - Tapes were self-administered - Homework on functionally assigned relevant activities was given | ||||
| Riccio et al., | Randomized single-blind cross-over study | Primary outcome measure:
- MI (upper limb) - AFT (FAS and time in s) | Group B improved statistically significantly more on all tests at the in-between-assessment | - | |
| N total: 36 | Both groups:
- 6 wk intervention period conventional neurorehabilitation 5×/wk, 3 h/day | Timing:
- Pre-test, in-between-assessment 3 wk (before cross-over) and post-test 6 wk after the start of the intervention - No follow-up | At post-test, after group A received MP too, no differences between groups existed anymore | ||
| N (GA): 18 | |||||
| N (GB): 18 | |||||
| Mean age (years):
GA: 60.17 (range 34–75) GB: 60.06 (range 32–75) | Experimental group A:
- First 3 weeks only conventional neurorehabilitation - Second 3 weeks MP: 1×/wk 60 min (twice a day 30 min) - MP in a separate quiet room involved relaxation and listening to an audio CD - Activities of the upper limbs, like placing the forearm on the table, were imagined - Kinaesthetic imagery was used | ||||
| Mean time post-stroke (weeks):
GA: 7.33 (range 4–12) GB: 7.44 (range 4–12) | Experimental group B:
- First 3 weeks MP: 1×/wk 60 min (twice a day 30 min) - MP in a separate quiet room involved relaxation and listening to an audio CD - Activities of the upper limbs, like placing the forearm on the table, were imagined - Kinaesthetic imagery was used - Second three weeks only conventional neurorehabilitation | ||||
| Bovend'Eerdt et al., | Single blind randomized controlled trial | MP | Primary outcome measure:
- Goal attainment scale | No conclusion:
Compliance of therapists and patients was too low | - |
| N total: 30 | Both groups:
- Standard physical- and occupational therapy as usual - 5 weeks intervention period - Homework: from the second half of the intervention period both groups were encouraged to practice at home for at least 5 min/day | Secondary outcome measure:
- BI - RMI - TUG - NEADL - ARAT - A custom-developed questionnaire (Imagery Questionnaire) on patient's confidence and perceived effort | |||
| N (EG): 15 | |||||
| N (CG): 15 | |||||
| Mean age, SD (years):
EG: 62.3 ± 11.75 CG: 50.6 ± 16.48 | Experimental group:
- MP integrated in therapy - At least 3×/week for first 2 weeks and 2×/weeks for the last 2 weeks (total time imagery ~6.5 h) - A framework for imagery was used - Therapists were trained to teach and monitor MP - Kinaesthetic and visual imagery were used | ||||
| Mixed population:
- Stroke: 14 (EG)/14 (CG) - TBI: 0 (EG)/1 (CG) - MS: 1 (EG)/0 (CG) | Control group:
- Therapy as usual - Control for attention (same dose) | Timing:
- Pre-test, post-test 6 wk after the start of the intervention - Follow-up 12 wk after the start of the intervention | |||
| Mean time since onset, SD (weeks):
EG: 15.9 ± 17.25 CG: 21.8 ± 15.17 | |||||
| Ietswaart et al., | Randomized controlled trial | Primary outcome measure:
- ARAT | No effects were found on any outcome measure | – | |
| N total: 121 | All groups:
- Therapy as usual - 4 weeks of intervention period, 3×/wk 45 min | Secondary outcome measure:
- Grip strength, hand-function - BI - Dynamometer, manual dexterity performance - Modified functional limitation profile | An added mental practice intervention has similar effects a controlled therapy as usual | ||
| N (EG): 39 | |||||
| N (placebo CG): 31 | |||||
| N (normal care CG): 32 | |||||
| Mean age (years):
EG: 69.3 Placebo CG: 68.6 Normal care CG: 64.4 | Experimental group:
- MP: 45 min; 30 min actively imagining (elementary movements, ADL), 10 min active motor imagery (using mirrors and videos), 5 min for a covert form of motor imagery activity (mentally rotating pictures of hands) - Kinaesthetic imagery was used | ||||
| Mean time post-stroke, SD (days):
EG: 80.2 ± 55.0 Placebo CG: 90.8 ± 63.4 | Attention-placebo control group:
- Placebo: 40 min; 25 min active visual and sensory imagery, 10 min cognitive inhibition, 5 min watching optical illusions of motion - Control for attention (same dose) | Timing
- Pre-test, post-test 5 wk after baseline - No Follow-up | |||
| Normal care CG: 80.5 ± 62.7 | Normal care control group:
- Therapy as usual | ||||
| Welfringer et al., | Randomized controlled trial | MP | Primary outcome measure:
- Neglect tests: bells cancellation test, drawing test, and text-reading task | MP had significant effects for the drawing test and the sensation functions only | Negative reported side-effect:
- diminished concentration capacity and signs of tiredness at the end training sessions |
| N total: 30 | Both groups:
- Standardized rehabilitation 4×/wk, 45 min - 3 weeks intervention period | ||||
| N (EG): 15 | |||||
| N (CG): 15 | |||||
| Mean age, SD (years):
EG: 56.3 ± 11.2 CG: 57.1 ± 11.3 | Experimental group:
- MP added to therapy - Two daily half-hour sessions (total 28–30 sessions) - Relaxation, followed by mental practice of positions of the contralesional upper limb: four positions and six sequences (simple and complex movements) - Each exercise up to 10 repetitions - Kinaesthetic imagery was used | Secondary outcome measures:
- Representation test (adapted): R-MIQ - Arm-Hand-Function tests: ARAT and sensation functions | Overall test results ambiguous | ||
| Self-perceived benefits of patients high | Positive reported side-effects:
- all patients reported sensations in the left arm during imagery - increased awareness of the left arm | ||||
| Mean time post-stroke, SD (months): | General effort to complete a MP session: NRS (1–10) | ||||
| EG: 3.2 ± 1.5 | Control group:
- No supplementary intervention | Timing:
- Pre-test, post-test 3 wk after the start of the intervention - No follow-up | |||
| CG: 3.4 ± 2.8 | |||||
| Braun et al., | Multicentre randomized controlled trial | Primary outcome measure:
- Numeric Rating Scale (1-10): patients' and therapists' perceived effect on performance of daily activities | No differences between groups short or long-term | Positive side-effect:
- Increased feeling of autonomy | |
| N total: 36 | Both groups:
- 6 wk intervention period - 6 wk physical therapy; according Dutch multidisciplinary guidelines for stroke rehabilitation - Task: drinking from a cup, walking (standardized) - Optional tasks: self-selected arm and leg activities | Secondary outcome measure:
- MI - NHPT - BBS - BI - 10 m-walking test - RMI | An embedded mental practice intervention in therapy as usual in nursing home residents has similar effects as therapy as usual in which there was control for attention | Negative side-effect:
- MP costs too much effort to perform (drop out) | |
| N (EG): 18 | |||||
| N (CG): 18 | |||||
| Mean age, SD (years):
EG: 77.7 ± 7.2 CG: 77.9 ± 7.4 | Experimental group:
- MP: 6 wk, 5×/wk 30 min - MP was given according to a 4-step framework involving explaining and developing imagery techniques before applying them - Visual and/or kinaesthetic imagery (patients' preference) was used | ||||
| Mean time post-stroke, SD (weeks):
EG: 6.1 ± 2.7 CG: 4.8 ± 3.3 | Control group:
- Therapy as usual - Control for attention: homework (same dose) | Timing:
- Pre-test, post-test 6 wk after the start of the intervention - Follow-up 6 months after the start of the intervention | |||
| Schuster et al., | Randomized controlled trial | Primary outcome measure:
- Time difference in seconds to perform the motor task from pre- to post-intervention | No between group differences were found | Logs were used but showed no side-effects or effects outside of the physical domain | |
| N total: 39 | Both groups:
- 2 weeks of intervention period - physiotherapy: 6 sessions 25–30 min | Secondary outcome measures:
- Help needed to perform the task using CMSA | A mental practice intervention embedded in or added to therapy as usual has similar effects as therapy as usual | ||
| N (EG1): 13 | |||||
| N (EG2): 12 | |||||
| N (CG): 14 | |||||
| Mean age, SD (years):
EG1: 65.8 ± 10.2 EG2: 59.7 ± 13.0 CG: 64.4 ± 6.8 | Experimental 1 group (embedded):
- MP was embedded in the six sessions - Total intervention time: 45–50 min - PETTLEP-framework was used; physical/emotion, timing, environment, task/learning/perspective - Complete motor task was divided into its 13 stages - Each part was imagined5× before physical performance - Kinaesthetic and visual imagery were used | Achieved stage of motor task
- BI - BBS - Computer-based Imaprax questionnaire - KVIQ - Activities-Specific Balance Confidence Scale, | |||
| Mean time post-stroke, SD (years):
EG1: 2.9 ± 1.9 EG2: 4.3 ± 3.6 CG: 3.5 ± 3.9 | Experimental 2 group (added):
- MP by tape: 3.5 min relaxation, 14.5 min MP, 2 min refocusing. - Total intervention time: 45–50 min - Kinaesthetic and visual imagery were used | intrinsic motivation evaluated in patient's diary | |||
| Control group:
- Physiotherapy - Control for attention: tape; 17 min; 3.5 min relaxation, 11.5 min information about stroke, 2 min refocusing | Timing:
- Twice at baseline, before intervention, post-test 2 wk after the start of the intervention - Follow-up after 2 wk | ||||
| Tamir et al., | Randomized controlled trial | Primary outcome measure:
- TUG | MP had significant differences in
- TUG - Getting up from a chair or from a supine lying position - Number of steps taken to complete the turn | Cognitive level: + Significant differences in
- Stroop test part B indicating an increase in attention and concentration | |
| N total: 23 | Both groups:
- 12 wk intervention period, 2×/wk 60 min physical therapy - Protocol of 3 parts (each 15–20 min): (1) callisthenic exercises (2) crucial motor tasks and (3) relaxation exercises - Emphasis on improving the smooth performance of tasks | Secondary outcome measures:
- Standing up and laying down - Turning in place 360° - Tandem stance | |||
| N (EG): 12 | |||||
| N (CG): 11 | |||||
| Mean age, SD (years):
EG: 67.4 ± 9.7 CG: 67.4 ± 9.1 | Experimental group:
- MP was performed within the second part of the protocol (crucal motor tasks) and during the relaxation period (previously practiced tasks were rehearsed mentally) - Kinaesthetic and visual imagery were used | - Functional reach and shoulder tug - UPDRS | - UPDRS section mental (between group-differences) | (clinical relevance unknown as same amount of improvement in both groups, but an increase in test errors in 4 subjects of the control contrary to 1 in the experimental group) | |
| Cognitive tasks:
- Clock drawing - Stroop test (part A and B) | |||||
| Mean duration of PD, SD (years):
EG: 7.4 ± 3.1 CG: 7.8 ± 4.5 | Control group:
- The exercises were performed physically and relaxation exercises were executed (control for attention, same dose) | Timing:
- Pre-test, post-test 12 wk after the start of the intervention - No follow-up | Some indication that imagery might increase motivation and arousal and reduce depression | ||
| Braun et al., | Multicentre randomized controlled trial | MP | Primary outcome measure:
- VAS (walking performance), patients' and therapists' perceived effect on performance | No differences between groups at short- or long-term | Negative side-effect:
- MP costs too much effort to perform (drop out) - Thinking about motor actions is too confronting (drop out) |
| N total: 47 | Both groups:
- 6 wk intervention period - Physical therapy; 1×/wk 60 min (groups) or 2×/wk 30 min (individuals), according Dutch guidelines for PD - Task: locomotor tasks (walking, standing up from the floor or a chair) | An embedded mental practice intervention in therapy as usual has similar effects as therapy as usual with relaxation | |||
| N (EG): 25 | Secondary outcome measures:
- TUG - 10 m walk test | ||||
| N (CG): 22 | |||||
| Mean age, SD (years):
EG: 70 ± 8 CG: 69 ± 8 | Experimental:
- MP: 1×/wk 20 min (groups) or 2×/wk 10 min MP (individuals) - MP was given according to a 4-step framework involving explaining and developing imagery techniques before applying them - Visual and/or kinaesthetic imagery (patients' preference) was used | Timing:
- Pre-test, post-test 6 wk after the start of the intervention - Follow-up 12 wk after the start of the intervention | |||
| Mean duration of PD, SD (years):
EG: 5.2 ± 5.0 CG: 6.6 ± 7.8 | |||||
| Control group:
- Control: therapy as usual - Control for attention: progressive relaxation (Jacobson, same dose) | |||||
Activities of Daily Living
Arm Functional Test
Action Research Arm Test
Berg Balance Scale
Barthel Index
Control Group
Chedoke-McMaster Stroke Assessment
Color Trails Test
Experimental Group
Functional Ability Scale
Fugl-Meyer assessment
hours
minutes
Kinesthetic and Visual Imagery Questionnaire
Motor Activity Log
Motricity Index
mental practice
Nottingham Extended Activities of Daily Living
Nine Hole Peg Test
Numeric Rating Scale
Occupational Therapy
Physiotherapy
Rivermead Mobility Index
Revised-Movement Imagery Questionnaire
Standard Deviation
Timed Up and Go
Unified Parkinson's disease Rating Scale
Visual Analogue Scale
weeks.
Overview of used measure instruments that could potentially be used in pooling.
Action Research Arm Test
Numeric Rating Scale/Likert Scale
Motricity Index
Berg Balance Scale
Barthel Index
10 m walking test
Rivermead Mobility Index
Timed Up and Go.
Gray Shading: Data could be pooled.