This information
collection is approved through 12/92 with the followi conditions:
1) CDC shall conduct a study subsequent to the proposed "pilot"
study to test the new training materials and protocols (refined as
a result of the data collected in the proposed study) against the
original training and protocols. 2) Because the purpose of the
proposed study is to "gather information about provider
acceptability and usability of the PACE training materi and
provider, office staff, and patient acceptability of the counselin
protocols", CDC shall eliminate the following questions that do not
re flect this purpose: **REMARKS CONTINUED**
Inventory as of this Action
Requested
Previously Approved
12/31/1992
12/31/1992
960
0
0
552
0
0
0
0
0
THE DATA COLLECTIONS WILL INCLUDE THE
PHYSICIAN'S PERSONAL PHYSICAL ACTIVITY HABITS, CURRENT HEALTH
PROMOTION ACTIVITIES, AND ACTIVITY COUNSELING PRACTICES.
RESPONDENTS INFORMATION WILL BE FROM OFFICE STA OF THE PHYSICIANS
AND TELEPHONE SURVEYS OF RANDOMLY SELECTED PATIENTS THAT WERE SEEN
BY THE PHYSICIAN DURING THE 6-MONTH PILOT. THE INFORMATION WILL BE
USED TO EVALUATE THE PHYSICIAN ASSESSMENT AND
On behalf of this Federal agency, I certify that
the collection of information encompassed by this request complies
with 5 CFR 1320.9 and the related provisions of 5 CFR
1320.8(b)(3).
The following is a summary of the topics, regarding
the proposed collection of information, that the certification
covers:
(i) Why the information is being collected;
(ii) Use of information;
(iii) Burden estimate;
(iv) Nature of response (voluntary, required for a
benefit, or mandatory);
(v) Nature and extent of confidentiality; and
(vi) Need to display currently valid OMB control
number;
If you are unable to certify compliance with any of
these provisions, identify the item by leaving the box unchecked
and explain the reason in the Supporting Statement.