Skip to main content
Download PDF

Effectiveness of calf muscle stretching for the short-term treatment of plantar heel pain: a randomised trial

BMC Musculoskeletal Disorders volume 8, Article number: 36 (2007) Cite this article

Abstract

Background

Plantar heel pain is one of the most common musculoskeletal disorders of the foot and ankle. Treatment of the condition is usually conservative, however the effectiveness of many treatments frequently used in clinical practice, including stretching, has not been established. We performed a participant-blinded randomised trial to assess the effectiveness of calf muscle stretching, a commonly used short-term treatment for plantar heel pain.

Methods

Ninety-two participants with plantar heel pain were recruited from the general public between April and June 2005. Participants were randomly allocated to an intervention group that were prescribed calf muscle stretches and sham ultrasound (n = 46) or a control group who received sham ultrasound alone (n = 46). The intervention period was two weeks. No participants were lost to follow-up. Primary outcome measures were 'first-step' pain (measured on a 100 mm Visual Analogue Scale) and the Foot Health Status Questionnaire domains of foot pain, foot function and general foot health.

Results

Both treatment groups improved over the two week period of follow-up but there were no statistically significant differences in improvement between groups for any of the measured outcomes. For example, the mean improvement for 'first-step' pain (0–100 mm) was -19.8 mm in the stretching group and -13.2 mm in the control group (adjusted mean difference between groups -7.9 mm; 95% CI -18.3 to 2.6). For foot function (0–100 scale), the stretching group improved 16.2 points and the control group improved 8.3 points (adjusted mean difference between groups 7.3; 95% CI -0.1 to 14.8). Ten participants in the stretching group experienced an adverse event, however most events were mild to moderate and short-lived.

Conclusion

When used for the short-term treatment of plantar heel pain, a two-week stretching program provides no statistically significant benefit in 'first-step' pain, foot pain, foot function or general foot health compared to not stretching.

Peer Review reports

Background

Plantar heel pain (plantar fasciitis) can be a painful and debilitating condition. It is highly prevalent with one recent United States study estimating that one million patient visits each year at office-based physicians and hospital outpatient departments are for the diagnosis and treatment of plantar heel pain [1]. The disorder appears in sedentary populations [2–4] with seven percent of adults aged 65 years or older found to have plantar heel pain [2, 3]. It also makes up one quarter of all foot injuries in runners [5] and up to 8% of all injuries to people participating in sporting activities [6–8]. It is the third most common running injury behind patellofemoral pain and iliotibial band friction syndrome [9]. The condition is thought to be multifactorial in origin with factors such as increased age, decreased ankle and first metatarsophalangeal joint range of motion, obesity and excessive periods of weight-bearing activity commonly suggested to be involved [10, 11].

A wide variety of management strategies have been developed to treat the disorder. A systematic review [12] identified 26 different conservative treatments that have been recommended for the treatment of plantar heel pain. At the time of the review, only heel pads, orthoses, steroid injections, night splints and extracorporeal shock wave therapy had been evaluated in randomised trials. The review found that although there is limited evidence for the effectiveness of local corticosteroid therapy, the effectiveness of other frequently employed treatments in altering the clinical course of plantar heel pain had not been established.

One of the more common conservative treatments for plantar heel pain is foot orthoses [13], however due to the manufacturing process there is often a period of a few weeks between the initial consultation and issuing the devices. As such, short-term treatments such as muscle stretches are regularly used to alleviate symptoms during this interim period. A recent systematic review [14] of randomised trials examined the effect of calf muscle stretching on ankle range of motion and found that stretching produces a small but statistically significant increase in ankle range of motion. Such an increase may reduce the symptoms of plantar heel pain by reducing the strain in the plantar fascia that the calf muscle places on it during standing and ambulation [15, 16]. However, it is unclear whether a change in ankle range of motion translates to a clinically relevant outcome for patients.

There have been no randomised controlled trials that have examined the effectiveness of calf muscle stretching per se. Two previous randomised controlled trials have compared two active stretching interventions for plantar heel pain: calf stretching compared with plantar fascia stretching [17] and sustained calf stretching compared with intermittent stretching [18]. Neither trial included a sham or no treatment control group, so the effect of calf muscle stretching by itself has not been examined. We conducted a randomised sham-controlled trial to determine whether calf muscle stretching is an effective short-term treatment for plantar heel pain.

Methods

A randomised, participant-blinded trial was conducted between April and June 2005. Participants with a clinical diagnosis of plantar heel pain and who provided informed consent were randomly allocated to one of two groups: (i) an intervention group receiving calf muscle stretching with sham ultrasound, or (ii) a control group receiving sham ultrasound only. Participants were informed prior to entering the study that a sham intervention was being administered in the trial and were blinded as to whether they received active treatment (i.e. stretching) or not. Ethical approval for the trial was gained from the University of Western Sydney Human Research Ethics Committee.

Participants

Participants were included if diagnosed with plantar heel pain defined as (i) localised pain at the plantar heel; (ii) that was worst when first standing or walking after rest; and (iii) that improved initially after first standing but worsened with increasing activity. As plantar heel pain is diagnosed clinically the majority of the time, we chose to not use expensive imaging procedures for diagnosis; thus maximising generalisability of our findings to standard clinical practice. Participants also needed to be 18 years of age or older and have had symptoms for four weeks or longer. Patients were excluded from the trial if patient history revealed any inflammatory, osseous, metabolic or neurological abnormalities. They were also excluded if they had received a corticosteroid injection within the past three months. Participants were encouraged not to commence use of any new treatments during the trial (e.g. anti-inflammatory medication, foot orthoses etc.).

Clinical protocol

Participants were recruited from local community newspaper advertisements in Campbelltown (Sydney, Australia) and treated at a university podiatry clinic. The random allocation sequence was generated using a computer program (Microsoft Excel) in one block (i.e. simple randomisation). The allocation sequence was concealed from the researcher (JR) enrolling and assessing participants in sequentially numbered, opaque, sealed and stapled envelopes. Aluminium foil inside the envelope was used to render the envelope impermeable to intense light. To prevent subversion of the allocation sequence, the name and date of birth of the participant was written on the envelope and a video tape made of the sealed envelope with participant details visible. Carbon paper inside the envelope transferred the information onto the allocation card inside the envelope and a second researcher (CC) later viewed video tapes to ensure envelopes were still sealed when participants' names were written on them. Corresponding envelopes were opened only after the enrolled participants completed all baseline assessments and it was time to allocate the intervention.

Three minutes of sham ultrasound (Accusonic AS250, Metron) was then given to the painful heel regardless of whether participants had been allocated the active intervention (i.e. stretching) or not. The ultrasound unit was powered with all operational lights activated. At commencement of treatment the researcher (JR) increased the wattage of the machine which was accompanied by 'beeping' sounds. However, no ultrasound was emitted as the internal timer was not activated (an external timer was used instead).

Participants in the stretching group were then given a wooden stretching wedge (Figure 1) on which to perform all stretches. This wedge was used to standardise the stretching technique across participants. The stretching technique was to be performed while standing. Participants were instructed to move their forefoot up the wedge until a stretch could be felt in the calf muscle while keeping their heel on the ground. They were advised to stretch the muscle for at least 5 minutes a day (a daily journal of their stretching was kept by all participants). They were permitted to stretch in smaller sessions (e.g. 1 minute) as long as a total of at least 5 minutes a day was achieved. Participants were warned not to overstretch the muscle and to reduce the force of the stretch by lowering their foot down the wedge if pain was felt in the calf muscle while stretching. Advice was given to stretch every day until the follow-up appointment 14 days later. Participants were not given any further instruction until the end of the trial. To assist with blinding, participants exited the building by a different doorway to the one through which they entered, thus minimising the likelihood of contact with other trial participants.

Figure 1
figure1

Stretching wedge.

Full size image

Outcome assessment was performed at baseline and 14 days. Baseline variables that were collected included age, sex, weight, self-reported hours on feet and duration of symptoms. Primary outcome measures were 'first-step' pain – the pain experienced when first standing after arising from bed in the morning – measured on a 100 mm Visual Analogue Scale and the Foot Health Status Questionnaire which has four domains covering foot pain, foot function, footwear and general foot health (although we pre-specified that we would not analyse the footwear domain). The Foot Health Status Questionnaire has been previously validated (content, criterion and construct validity) across a wide spectrum of pathologies including skin, nail and musculoskeletal disorders. It has a high test-retest reliability (intraclass correlation coefficients ranging from 0.74 to 0.92) and a high degree of internal consistency (Cronbach's α ranging from 0.85 to 0.88) [19]. Both measures are self-administered; however to minimise the investigator having influence on participant responses, participant-completed outcome assessments were performed prior to each consultation.

Secondary outcome measures were ankle range of motion and foot posture. Weight-bearing ankle dorsiflexion (a measure of ankle joint tightness) was measured using the Lunge Test [20] which is reported to also have high intra-rater (intraclass correlation coefficient 0.98) and inter-rater reliability (intraclass correlation coefficient 0.97). Foot posture (e.g. whether someone has a low- or high-arched foot) was measured using the Foot Posture Index (FPI-6) which is reported to have high internal consistency (Cronbach's α 0.83) and high test-retest reliability (intraclass correlation coefficients ranging from 0.62 to 0.91) [21]. The researcher completing follow-up measurement of ankle dorsiflexion and foot posture was not blinded to participant allocation.

Sample size, data handling and analysis

The sample size of 92 (i.e. 46 per group), calculated a priori, was based upon the ability to detect a minimal important difference of 10 mm [22–24] on the Visual Analogue Scale (standard deviation 17) between groups with 80% probability and alpha level of 0.05. This sample size also provided adequate power to detect a minimal important difference between groups of 12 points on the pain domain of the Foot Health Status Questionnaire (standard deviation 20). We conservatively ignored the extra precision provided by the covariate analysis when estimating sample size.

Independent researchers (not otherwise involved in the trial – see acknowledgments) performed data entry and were blinded to group allocation. Double data entry was used to check for errors. Statistical analyses were performed while researchers were blinded to group allocation.

An independent sample t-test was used to determine if there was a difference between groups in the number of days between baseline and follow-up appointments. Outcome data were analysed by intention to treat and according to a pre-planned protocol (i.e. a priori). To maximise precision of estimates, analysis of covariance (ANCOVA) was conducted using a linear regression approach [25, 26]. The primary outcomes analysed were the change in 'first-step' pain (Visual Analogue Scale), foot pain, foot function and general foot health (Foot Health Status Questionnaire). Secondary outcomes included ankle range of motion (Lunge Test) and foot posture (FPI-6). We pre-specified that the baseline outcome measure would be used as the only covariate in each analysis [27] therefore for each of the primary and secondary outcomes we adjusted for the outcome at baseline.

Participants were also asked which intervention (active, sham or don't know) they thought they had received and an index [28] calculated to assess the success of blinding. The index takes the value 1 for complete blinding and 0 for complete lack of blinding; 0.5 is the equivalent of random guessing.

Results

The flow of participants through the trial is shown in Figure 2. There were no participants lost to follow-up. Baseline characteristics (Table 1) of both groups were similar although the control group had less women 25 (54%) versus 31 (67%) and were on their feet slightly longer each day (mean 9.1 SD ± 3.7 hours versus mean 7.5 SD ± 3.5 hours).

Figure 2
figure2

Participant flow diagram.

Full size image
Table 1 Baseline characteristics of participants. Values are means (± standard deviation) unless stated otherwise.
Full size table

Participants in the stretching group stretched for a median of 14 days (range 5 to 16 days). There was no difference between the groups in time to follow-up (p = 0.489). The median time between baseline and the review appointment was 14 days (range 13 to 16) for the stretching group and 14 days (range 13 to 15) for the control group.

Both the stretching and control group improved in 'first-step' pain, foot pain, foot function and general foot health over the two weeks of follow-up. When compared to the control group, the stretching group demonstrated a small improvement in 'first-step' pain (ANCOVA-adjusted mean difference between groups: -7.9 mm; 95% CI -18.3 to 2.6) and foot function (ANCOVA-adjusted mean difference between groups: 7.3; 95% CI -0.1 to 14.8) but these were not statistically significant. Similarly there were no statistically significant differences between groups for any of the other primary or secondary outcomes (Tables 2 and 3).

Table 2 Primary outcomes at baseline and follow-up.
Full size table
Table 3 Secondary outcomes at baseline and follow-up.
Full size table

Ten participants (22%) in the stretching group experienced adverse events: increased heel pain while stretching (n = 4), calf pain (n = 4), and a new pain in lower limb (n = 2). Adverse events were recorded as mild (n = 4), moderate (n = 2) or severe (n = 4) in nature. One participant discontinued treatment after 5 days of stretching due to severe heel pain while stretching. Upon cessation of stretching, all adverse events resolved. There were no adverse events reported in the control group.

With respect to blinding, thirty-six participants (78%) in the stretching group correctly identified their treatment group compared with twelve participants (26%) in the control group. Seven participants (15%) in the stretching group were uncertain which treatment they received, compared with twelve participants (26%) in the control group. Three participants (7%) in the stretching group and twenty-two participants (48%) in the control group incorrectly identified their treatment group. The blinding index was 0.49 (bootstrap 95% confidence interval 0.39 to 0.57; p < 0.001) interpreted as moderate success of blinding.

Discussion

The results demonstrate that calf muscle stretching over a two-week period produces no statistically significant beneficial effects for foot pain and general foot health compared with not stretching. Although there was a trend for greater improvement in the stretching group in 'first-step' pain (by approximately 8 points on the 100 point Visual Analogue Scale) and foot function (by approximately 7 points on the 100 point Foot Health Status Questionnaire) these were also not statistically significant. In regards to foot function, no minimal important difference is known for the outcome and therefore the trial may have been underpowered to detect a statistically significant difference. Further, no differences were found in secondary outcomes of ankle range of motion and foot posture.

Participant characteristics in this trial were similar to samples in previous heel pain trials [13, 29–31]. Participants were primarily middle-aged, overweight and spent the majority of the day on their feet. Likewise, participants also presented with relatively chronic symptoms.

The majority of adverse events in this trial were described by participants as short-lived and mild to moderate in intensity. Only one participant discontinued stretching due to an adverse event. Four events were due to increased pain while stretching, another four were due to calf pain and two due to a new pain in the lower limb. Participants noticed that the use of the wooden wedge placed increased pressure under the heel as the position of the foot on the wedge during the stretching procedure redistributed force away from the forefoot to the plantar heel region. This could have led to the four participants reporting increased pain while stretching. Caution should therefore be used in instructing participants to stretch their calf muscles by raising their forefoot from the ground (e.g. on a book or wedge similar to the one used in this trial). While we chose this form of stretching because it standardised the stretching technique across participants, alternative stretching methods that do not place increased pressure on the plantar heel (e.g. lowering the heel while the forefoot is on a step) may avoid such an adverse event.

The findings of this trial need to be viewed in light of some limitations. Firstly, the evidence from this trial is for one particular technique of stretching the calf muscle. Although participants reported being able to feel a stretch, no increase in ankle range of motion was found. Other stretching techniques such as lunges (dynamic stretching), proprioceptive neuromuscular facilitation, or using splints (e.g. night stretching splints) may yield other results. The stretching technique we utilised – using a wooden wedge – ensured a suitable stretch was applied in a relatively controlled manner. Secondly, the trial specifically examined the effect of stretching over a two-week period as a short-term treatment for plantar heel pain; generally the period a patient waits for the fabrication of a longer-term treatment such as foot orthoses [29]. It would be of interest to evaluate the effectiveness of regular stretching over a longer period to investigate whether the intervention has a long-term effect. This may obviate the need to institute more expensive long-term treatments such as foot orthoses; although the risk of a higher incidence of adverse events may not make this worthwhile.

This is the first randomised trial to examine the effect of calf stretching compared with no stretching for plantar heel pain. Two previous randomised trials have examined two different stretching techniques for plantar heel pain without inclusion of a non-stretching control group [17, 18]. DiGiovanni et al [17] compared calf muscle stretching with plantar fascia tissue stretches over eight weeks. Both groups experienced reductions in pain, however the plantar fascia stretches were found to provide a statistically significant greater reduction in pain when compared to the calf muscle stretches. Porter et al [18] compared sustained 3 minute calf stretches with intermittent 20 second calf stretches for plantar heel pain and found no significant differences in improvement between groups. However, without a sham or no stretching control group, it is not possible to attribute the observed improvements in either trial to the stretching. In view of the favourable natural history of plantar heel pain participants in the trial may have improved irrespective of treatment due to the spontaneous resolution of the condition or as a result of the placebo or Hawthorne effects. Our trial clearly addresses this limitation and represents a more precise estimate of the true effect of calf muscle stretches for plantar heel pain.

Conclusion

When used for the short-term treatment of plantar heel pain, stretching for two weeks provides no statistically significant improvements in 'first-step' pain, foot pain, foot function and general foot health compared with a control group. It was also associated with mild to moderate short-lived adverse events. Based upon our results a program of calf muscle stretching, similar to that conducted in this trial, is not recommended for plantar heel pain.

References

  1. 1.

    Riddle DL, Schappert SM: Volume of ambulatory care visits and patterns of care for patients diagnosed with plantar fasciitis: a national study of medical doctors. Foot Ankle Int. 2004, 25 (5): 303-310.

    PubMed  Google Scholar 

  2. 2.

    Dunn JE, Link CL, Felson DT, Crincoli MG, Keysor JJ, McKinlay JB: Prevalence of foot and ankle conditions in a multiethnic community sample of older adults. Am J Epidemiol. 2004, 159 (5): 491-498. 10.1093/aje/kwh071.

    CAS  Article  PubMed  Google Scholar 

  3. 3.

    Badlissi F, Dunn JE, Link CL, Keysor JJ, McKinlay JB, Felson DT: Foot musculoskeletal disorders, pain, and foot-related functional limitations in older persons. J Am Geriatr Soc. 2005, 53 (6): 1029-1033. 10.1111/j.1532-5415.2005.53315.x.

    Article  PubMed  Google Scholar 

  4. 4.

    Buchbinder R: Plantar fasciitis. N Engl J Med. 2004, 350 (21): 2159-2166. 10.1056/NEJMcp032745.

    CAS  Article  PubMed  Google Scholar 

  5. 5.

    Clement DB, Taunton JE, Smart GW, McNicol KL: A survey of overuse running injuries. Phys Sportsmed. 1981, 9 (5): 47-58.

    Google Scholar 

  6. 6.

    James SL, Bates BT, Osternig LR: Injuries to runners. Am J Sports Med. 1978, 6 (2): 40-50.

    CAS  Article  PubMed  Google Scholar 

  7. 7.

    Lysholm J, Wiklander J: Injuries in runners. Am J Sports Med. 1987, 15 (2): 168-171.

    CAS  Article  PubMed  Google Scholar 

  8. 8.

    Agosta J: Epidemiology of a podiatric sports medicine clinic. Aust Podiatrist. 1994, 28 (4): 93-96.

    Google Scholar 

  9. 9.

    Taunton JE, Ryan MB, Clement DB, McKenzie DC, Lloyd-Smith DR, Zumbo BD: A retrospective case-control analysis of 2002 running injuries. Br J Sports Med. 2002, 36 (2): 95-101. 10.1136/bjsm.36.2.95.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  10. 10.

    Riddle DL, Pulisic M, Pidcoe P, Johnson RE: Risk factors for plantar fasciitis: a matched case-control study. J Bone Joint Surg Am. 2003, 85-A (5): 872-877.

    PubMed  Google Scholar 

  11. 11.

    Irving DB, Cook JL, Menz HB: Factors associated with chronic plantar heel pain: a systematic review. J Sci Med Sport. 2006, 9 (1-2): 11-22. 10.1016/j.jsams.2006.02.004.

    CAS  Article  PubMed  Google Scholar 

  12. 12.

    Crawford F, Thomson C: Interventions for treating plantar heel pain. Cochrane Database Syst Rev. 2003, CD000416-3

  13. 13.

    Landorf KB, Keenan AM, Herbert RD: Effectiveness of three foot orthoses for plantar fasciitis: a randomised trial. Arch Intern Med. 2006, 166 (12): 1305-1310. 10.1001/archinte.166.12.1305.

    Article  PubMed  Google Scholar 

  14. 14.

    Radford JA, Burns J, Buchbinder R, Landorf KB, Cook C: Does stretching increase ankle dorsiflexion range of motion? A systematic review. Br J Sports Med. 2006, 40 (10): 870-875. 10.1136/bjsm.2006.029348.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  15. 15.

    Carlson RE, Fleming LL, Hutton WC: The biomechanical relationship between the tendoachilles, plantar fascia and metatarsophalangeal joint dorsiflexion angle. Foot Ankle Int. 2000, 21 (1): 18-25.

    CAS  PubMed  Google Scholar 

  16. 16.

    Erdemir A, Hamel AJ, Fauth AR, Piazza SJ, Sharkey NA: Dynamic loading of the plantar aponeurosis in walking. J Bone Joint Surg Am. 2004, 86-A (3): 546-52.

    PubMed  Google Scholar 

  17. 17.

    DiGiovanni BF, Nawoczenski DA, Lintal ME, Moore EA, Murray JC, Wilding GE, Baumhauer JF: Tissue-specific plantar fascia-stretching exercise enhances outcomes in patients with chronic heel pain. J Bone Joint Surg Am. 2003, 85-A (7): 1270-1277.

    PubMed  Google Scholar 

  18. 18.

    Porter D, Barrill E, Oneacre K, May BD: The effects of duration and frequency of Achilles tendon stretching on dorsiflexion and outcome in painful heel syndrome: a randomised, blinded, control study. Foot Ankle Int. 2002, 23 (7): 619-624.

    Article  PubMed  Google Scholar 

  19. 19.

    Bennett PJ, Patterson C, Wearing S, Baglioni T: Development and validation of a questionnaire designed to measure foot-health status. J Am Podiatr Med Assoc. 1998, 88 (9): 419-428.

    CAS  Article  PubMed  Google Scholar 

  20. 20.

    Bennell K, Talbot R, Wajswelner H, Techovanich W, Kelly D: Intra-rater and inter-rater reliability of a weight-bearing lunge measure of ankle dorsiflexion. Aust J Physiother. 1998, 44 (3): 175-180.

    Article  PubMed  Google Scholar 

  21. 21.

    Redmond AC, Crosbie J, Ouvrier RA: Development and validation of a novel rating system for scoring foot posture: the Foot Posture Index. Clinical Biomechanics. 2006, 21 (1): 89-98. 10.1016/j.clinbiomech.2005.08.002.

    Article  PubMed  Google Scholar 

  22. 22.

    Kelly AM: Does the clinically significant difference in visual analog scale pain scores vary with gender, age, or cause of pain?. Acad Emerg Med. 1998, 5 (11): 1086-1090.

    CAS  Article  PubMed  Google Scholar 

  23. 23.

    Powell CV, Kelly AM, Williams A: Determining the minimum clinically significant difference in visual analog pain score for children. Ann Emerg Med. 2001, 37 (1): 28-31. 10.1067/mem.2001.111517.

    CAS  Article  PubMed  Google Scholar 

  24. 24.

    Kelly AM: The minimum clinically significant difference in visual analogue scale pain score does not differ with severity of pain. Emerg Med J. 2001, 18 (3): 205-207. 10.1136/emj.18.3.205.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  25. 25.

    Vickers AJ, Altman DG: Statistics notes: Analysing controlled trials with baseline and follow up measurements. BMJ. 2001, 323 (7321): 1123-4. 10.1136/bmj.323.7321.1123.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  26. 26.

    Twisk J, Proper K: Evaluation of the results of a randomized controlled trial: how to define changes between baseline and follow-up. J Clin Epidemiol. 2004, 57: 223-228. 10.1016/j.jclinepi.2003.07.009.

    Article  PubMed  Google Scholar 

  27. 27.

    Raab GM, Day S, Sales J: How to select covariates to include in the analysis of a clinical trial. Control Clin Trials. 2000, 21 (4): 330-342. 10.1016/S0197-2456(00)00061-1.

    CAS  Article  PubMed  Google Scholar 

  28. 28.

    James KE, Bloch DA, Lee KK, Kraemer HC, Fuller RK: An index for assessing blindness in a multi-centre clinical trial: Disulfiram for alcohol cessation - a VA cooperative study. Stat Med. 1996, 15: 1421-1434. 10.1002/(SICI)1097-0258(19960715)15:13<1421::AID-SIM266>3.0.CO;2-H.

    CAS  Article  PubMed  Google Scholar 

  29. 29.

    Martin JE, Hosch JC, Goforth WP, Murff RT, Lynch DM, Odom RD: Mechanical treatment of plantar fasciitis: A prospective study. J Am Podiatr Med Assoc. 2001, 91 (2): 55-62.

    CAS  Article  PubMed  Google Scholar 

  30. 30.

    Landorf KB, Radford JA, Keenan AM, Redmond AC: Effectiveness of low-Dye taping for short-term management of plantar fasciitis. J Am Podiatr Med Assoc. 2005, 95 (6): 525-530.

    Article  PubMed  Google Scholar 

  31. 31.

    Pfeffer G, Bacchetti P, Deland J, Lewis A, Anderson R, Davis W, Alvarez R, Brodsky J, Cooper P, Frey C, Herrick R, Myerson M, Sammarco J, Janecki C, Ross S, Bowman M, Smith R: Comparison of custom and prefabricated orthoses in the initial treatment of proximal plantar fasciitis. Foot Ankle Int. 1999, 20 (4): 214-221.

    CAS  Article  PubMed  Google Scholar 

Pre-publication history

  1. The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2474/8/36/prepub

Download references

Acknowledgements

The authors would like to thank Jill Hackett and Kiel Latham for their assistance in completing double data entry and Associate Professor Andrew Forbes for his assistance with blinding statistical analysis. Funding for consumables used in the trial and data entry was assisted by the Australian Podiatry Education and Research Foundation, the New South Wales Podiatrists Registration Board, and Foot Science International Ltd. The researchers were completely independent from the foundations and company that assisted with funding the trial. The funding bodies had no role in study design; in the collection, analysis, and interpretation of data; in the writing of the manuscript; or in the decision to submit the manuscript for publication.

Author information

Affiliations

  1. School of Biomedical and Health Sciences, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW, 1797, Australia

    Joel A Radford & Catherine Cook

  2. Department of Podiatry, School of Human Biosciences, La Trobe University, Bundoora, Victoria, 3086, Australia

    Karl B Landorf

  3. Monash Department of Clinical Epidemiology at Cabrini Hospital and Department of Epidemiology and Preventive Medicine, Monash University, Malvern, Victoria, 3144, Australia

    Rachelle Buchbinder

Authors
  1. Joel A Radford
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Karl B Landorf
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Rachelle Buchbinder
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Catherine Cook
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to Joel A Radford.

Additional information

Authors' contributions

JAR conceptualised the trial, undertook a literature search, designed the trial, collected and analysed the data, interpreted the results and wrote the paper. JAR is guarantor of the paper. KBL assisted with the conceptualisation and design of the trial, analysis of the data, interpretation of the results and writing of the paper. RB assisted with the conceptualisation and design of the trial and writing of the paper. CC assisted with the planning of the project and writing of the paper. All authors have read and approved the final manuscript.

Authors’ original submitted files for images

Below are the links to the authors’ original submitted files for images.

Authors’ original file for figure 1

Authors’ original file for figure 2

Rights and permissions

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and Permissions

About this article

Cite this article

Radford, J.A., Landorf, K.B., Buchbinder, R. et al. Effectiveness of calf muscle stretching for the short-term treatment of plantar heel pain: a randomised trial. BMC Musculoskelet Disord 8, 36 (2007). https://doi.org/10.1186/1471-2474-8-36

Download citation

Keywords

  • Minimal Important Difference
  • Calf Muscle
  • Ankle Dorsiflexion
  • Extracorporeal Shock Wave Therapy
  • Plantar Fascia

BMC Musculoskeletal Disorders

ISSN: 1471-2474

Contact us