Pain is the most common symptom reported in the general population and the leading cause of work disability (
1,
2). Chronic pain reduces activities of daily living (ADL) and quality of life (QOL) and is a burden not only on the patient but also on family members and others involved (
3-
7). Musculoskeletal pain is also one of the major problems for Japan and its aging population since it requires assistance and leads to patients becoming bedridden. A national survey of 10,000 people conducted by a research group from the Ministry of health, labor and welfare in Japan showed that 15.4% of the population had chronic musculoskeletal pain when chronic pain was defined as 1; the presence of symptoms within the past month, 2; persistent pain for at least 6 months, and 3; a score of at least 5 on the visual analogue scale (VAS) (
8). The survey also revealed a high frequency of low satisfaction with treatment and doctor shopping in about half the population. Prolonged pain can lead to sleep disorders, decreased desire, anxiety, depression, decreased routine activity, occasionally causes withdrawal from society and otherwise disrupts daily activities (
9). As a result, patients with chronic pain fall into a vicious circle in which these psychological and social factors complicate their condition. In such cases, satisfactory treatment outcomes may be unachievable with a uniform therapeutic approach seeking only to eliminate pain. Often a multifaceted, collaborative (multidisciplinary) intervention is needed (
6,
7,
10,
11). In particular, therapeutic approaches based on cognitive behavioral therapy (CBT) under multidisciplinary approaches are recommended. Cognitive behavioral therapy seeks to deepen the understanding of one’s pain and teach self-control and coping strategies. Several studies recently reported that telecare collaborative managements substantially improved pain outcomes and secondary health-related QOL outcomes in patients suffering from pain (
2,
12,
13).
With funding from the Ministry of health, labor, and welfare of Japan, we were asked to found a nonprofit organization (NPO) offering peer support and education in pain management skills to people with pain, their family and friends, and health care professionals. We founded an NPO called the ‘Pain Medical Research and Information Center’ in 2011 and commenced a telephone-based consultation approach in order to offer education in pain management skills and guidance on activities of daily living partially based on a cognitive-behavioral approach to people with pain and their family.